Jing-Yu Guo, Rui-Han Dai, Wen-Cong Xu, Ruo-Xin Wu and Shi-Kai Tian*
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1 Electronic Supplementary Material (ESI) for ChemComm. This journal is The Royal Society of Chemistry 2018 TfNHNHBoc as a SCF 3 source in the sulfenylation of indoles Jing-Yu Guo, Rui-Han Dai, Wen-Cong Xu, Ruo-Xin Wu and Shi-Kai Tian* Hefei National Laboratory for Physical Sciences at the Microscale, Center for Excellence in Molecular Synthesis, and Department of Chemistry, University of Science and Technology of China, Hefei, Anhui , China Supporting information Table of contents General information...s-2 Preparation of TfNHNHCO2Et.. S-2 General procedure for the sulfenylation of indoles with TfNHNHBoc (Scheme 1)..S-2 Analytical data for the products shown in Scheme 1...S-3 Sulfenylation of pyrole 5 with TfNHNHBoc (eqn (1)) S-10 Mechanistic studies... S-11 References S-14 Copies of 1 H, 13 C and 19 F NMR spectra.. S-16 S-1
2 General information 1 H NMR and 13 C NMR spectra were recorded on a Bruker AC-400 FT spectrometer (400 MHz and 100 MHz, respectively) and were referenced internally with tetramethylsilane (δ H 0.00), CDCl3 (δ C 77.16), and acetone-d6 (δ H 2.05, δ C 29.84). 19 F NMR was recorded on a Bruker AC-400 FT spectrometer (376 MHz, CFCl3 as an external standard). Chemical shifts (δ) and coupling constants (J) were expressed in ppm and Hz, respectively. The following abbreviations are used in reporting NMR data: s, singlet; d, doublet; t, triplet; q, quartet; m, multiplet; br, broad. High resolution mass spectra (HRMS) were recorded on a LC-TOF spectrometer (Micromass). Electrospray ionization (ESI) mass spectrometry data were acquired using a Thermo LTQ Orbitrap XL instrument equipped with an ESI source and controlled by Xcalibur software. Melting points are uncorrected. Trifluoromethanesulfonyl hydrazides 2a and 2c-f were prepared according to literature procedures. 1 The rest of chemicals were purchased from the Sinopharm Chemical Reagent Co., Meryer, Acros, Alfa Aesar, Adamas, and TCI, and used as received. Abbreviations: Bn = benzyl, Boc = tert-butoxycarbonyl, Cbz = benzyloxycarbonyl, DCE = 1,2-dichloroethane, DMF = N,N-dimethylformamide, DMSO = dimethyl sulfoxide, TBHP = tert-butyl hydroperoxide, Tf = trifluoromethylsulfonyl, Ts = p-toluenesulfonyl. Preparation of TfNHNHCO 2 Et To a solution of triflic anhydride (5.64 g, 3.36 ml, 20.0 mmol) in dichloromethane (20 ml) was added dropwise to a mixture of EtO2CNHNH2 (2.08 g, 20.0 mmol) and triethylamine (2.23 g, 3.05 ml, 22.0 mmol) in dichloromethane (100 ml) under nitrogen at -78 o C. The mixture was allowed to warm to room temperature and stirred for 2 h, then washed twice with water, once with 5% aqueous hydrochloric acid, and once with water, dried over anhydrous sodium sulfate, and the solvent was evaporated in vacuum. The residue was purified by silica gel column chromatography, eluting with ethyl acetate/petroleum ether (4:1 v/v), to give TfNHNHCO2Et (2b) as a white solid (1.30 g, 28% yield). m.p C; 1 H NMR (400 MHz, CDCl3) δ 7.76 (s, br, 1H), 6.87 (s, br, 1H), 4.27 (q, J = 7.1 Hz, 2H), 1.31 (t, J = 7.1 Hz, 3H); 13 C NMR (100 MHz, CDCl3) δ 156.5, (q, J = Hz), 63.9, 14.3; 19 F NMR (376 MHz, CDCl3) δ ; HRMS (ESI) calcd for C4H8F3N2O4S + (M + H) , found General procedure for the sulfenylation of indoles with TfNHNHBoc (Scheme 1) To a reaction tube equipped with a magnetic stir bar was charged with TfNHNHBoc (2a) (211 mg, 0.80 mmol), indole 1 (0.40 mmol), and CuCl (4.0 mg, 10 mol%). The tube was sealed with a septum, evacuated, and backfilled with nitrogen three times. DMSO (31.2 mg, 28 μl, 0.40 mmol) and MeCN (2.0 ml) were added via syringe with gentle stirring. The reaction vessel was allowed to stir at 80 C for 10 h. The mixture was cooled to room temperature and purified directly by silica gel S-2
3 chromatography, eluting with ethyl acetate/petroleum ether (1:10~1:5 v/v), to give thioether 3. Analytical data for the products shown in Scheme 1 3-((Trifluoromethyl)thio)-1H-indole (3a) 2 was obtained in 80% yield (69.4 mg) as a yellow oil. 1 H NMR (400 MHz, CDCl3) δ 8.37 (s, br, 1H), (m, 1H), (m, 1H), (m, 1H), (m, 2H); 13 C NMR (100 MHz, CDCl3) δ 136.1, 132.9, (q, J = Hz), 129.5, 123.5, 121.7, 119.3, 111.9, 95.3 (q, J = 2.4 Hz); 19 F NMR (376 MHz, CDCl3) δ Methyl-3-((trifluoromethyl)thio)-1H-indole (3b) 3 was obtained in 64% yield (59.1 mg) as a yellow oil. 1 H NMR (400 MHz, CDCl3) δ 8.25 (s, br, 1H), 7.38 (s, 1H), (m, 2H), 6.97 (d, J = 6.0 Hz, 1H), 2.82 (s, 3H); 13 C NMR (100 MHz, CDCl3) δ 136.4, 134.2, 131.7, (q, J = Hz), 126.8, 123.5, 109.9, 95.0 (q, J = 2.4 Hz), 19.5; 19 F NMR (376 MHz, CDCl3) δ Methoxy-3-((trifluoromethyl)thio)-1H-indole (3c) 3 was obtained in 66% yield (65.2 mg) as a yellow oil. 1 H NMR (400 MHz, CDCl3) δ 8.44 (s, br, 1H), 7.31 (s, 1H), 7.16 (t, J = 8.0 Hz, 1H), 6.95 (d, J = 8.4 Hz, 1H), 6.62 (d, J = 8.0 Hz, 1H), 3.93 (s, 3H); 13 C NMR (100 MHz, CDCl3) δ 154.6, 138.0, 132.6, (q, J = Hz), 124.4, 118.6, 105.0, 102.2, 94.4 (q, J = 2.5 Hz), 55.6; 19 F NMR (376 MHz, CDCl3) δ ((Trifluoromethyl)thio)-1H-indol-4-ol (3d) 4 was obtained in 54% yield (50.2 mg) as a yellow oil. 1 H NMR (400 MHz, CDCl3) δ 8.64 (s, br, 1H), 7.42 (d, J = 2.0 Hz, 1H), 7.16 (t, J = 8.0 Hz, 1H), 6.98 (d, J = 8.0 Hz, 1H), (m, 2H); 13 C NMR (100 MHz, CDCl3) δ 150.6, 137.8, 132.9, (q, J = Hz), 125.2, 116.6, 107.2, 104.6, 91.5 (q, J = 2.4 Hz); 19 F NMR (376 MHz, CDCl3) S-3
4 δ Chloro-3-((Trifluoromethyl)thio)-1H-indole (3e) was obtained in 74% yield (74.7 mg) as a yellow oil. 1 H NMR (400 MHz, CDCl3) δ 8.63 (s, br, 1H), 7.53 (d, J = 2.8 Hz, 1H), 7.30 (d, J = 8.0 Hz, 1H), (m, 2H); 13 C NMR (100 MHz, CDCl3) δ 137.5, 135.1, (q, J = Hz), 126.8, 125.1, 124.1, 123.2, 110.8, 95.4 (q, J = 2.6 Hz); 19 F NMR (376 MHz, CDCl3) δ ; HRMS (ESI) calcd for C9H6ClF3NS + (M + H) , found Bromo-3-((trifluoromethyl)thio)-1H-indole (3f) 2 was obtained in 54% yield (64.2 mg) as a yellow oil. 1 H NMR (400 MHz, CDCl3) δ 8.59 (s, br, 1H), 7.55 (d, J = 1.2 Hz, 1H), 7.41 (d, J = 8.0 Hz, 1H), 7.35 (d, J = 8.0 Hz, 1H), 7.08 (t, J = 8.0 Hz, 1H); 13 C NMR (100 MHz, CDCl3) δ 137.2, 135.5, (q, J = Hz), 126.8, 126.1, 124.4, 114.4, 111.5, 96.3 (q, J = 2.6 Hz); 19 F NMR (376 MHz, CDCl3) δ Methyl 3-((trifluoromethyl)thio)-1H-indole-4-carboxylate (3g) was obtained in 71% yield (78.1 mg) as a yellow oil. 1 H NMR (400 MHz, CDCl3) δ 9.80 (s, br, 1H), (m, 1H), (m, 2H), 7.21 (t, J = 7.8 Hz, 1H), 4.02 (s, 3H); 13 C NMR (100 MHz, CDCl3) δ 169.7, 137.4, 136.2, (q, J = Hz), 125.6, 124.4, 123.3, 122.4, 115.9, 94.6 (d, J = 2.3 Hz), 52.3; 19 F NMR (376 MHz, CDCl3) δ ; HRMS (ESI) calcd for C11H9F3NO2S + (M + H) , found Methyl-3-((trifluoromethyl)thio)-1H-indole (3h) 2 was obtained in 68% yield (62.8 mg) as a yellow oil. 1 H NMR (400 MHz, CDCl3) δ 8.21 (s, br, 1H), 7.58 (s, 1H), 7.36 (d, J = 2.8 Hz, 1H), 7.22 (d, J = 8.4 Hz, 1H), 7.09 (dd, J = 8.4, 1.2 Hz, 1H), 2.47 (s, 3H); 13 C NMR (100 MHz, CDCl3) δ 134.4, S-4
5 133.0, 131.4, 129.8, (q, J = Hz), 125.2, 118.9, 111.5, 94.8 (q, J = 2.3 Hz), 21.6; 19 F NMR (376 MHz, CDCl3) δ Methoxy-3-((trifluoromethyl)thio)-1H-indole (3i) 2 was obtained in 76% yield (75.1 mg) as a yellow oil. 1 H NMR (400 MHz, CDCl3) δ 8.48 (s, br, 1H), 7.43 (d, J = 2.8 Hz, 1H), (m, 2H), 6.93 (d, J = 8.8 Hz, 1H), 3.89 (s, 3H); 13 C NMR (100 MHz, CDCl3) δ 155.6, 133.4, 131.0, 130.4, (q, J = Hz), 114.1, 112.7, 100.6, 95.0, 55.9; 19 F NMR (376 MHz, CDCl3) δ (Benzyloxy)-3-((trifluoromethyl)thio)-1H-indole (3j) was obtained in 52% yield (67.2 mg) as a yellow oil. 1 H NMR (400 MHz, CDCl3) δ 8.34 (s, br, 1H), 7.47 (d, J = 7.2 Hz, 2H), 7.37 (t, J = 7.2 Hz, 2H), (m, 3H), (m, 1H), 6.96 (dd, J = 8.8, 2.4 Hz, 1H), 5.10 (s, 2H); 13 C NMR (100 MHz, CDCl3) δ 154.7, 137.2, 133.6, 131.2, 130.3, (d, J = Hz), 128.7, 128.2, 128.0, 114.5, 112.8, 102.1, 94.8 (d, J = 2.3 Hz), 71.0; 19 F NMR (376 MHz, CDCl3) δ ; HRMS (ESI) calcd for C16H13F3NOS + (M + H) , found Fluoro-3-((trifluoromethyl)thio)-1H-indole (3k) 3 was obtained in 86% yield (81.2 mg) as a yellow oil. 1 H NMR (400 MHz, CDCl3) δ 8.47 (s, br, 1H), 7.51 (s, 1H), 7.43 (d, J = 9.2 Hz, 1H), 7.30 (dd, J = 8.8, 4.0 Hz, 1H), 7.01 (t, J = 9.2 Hz, 1H); 13 C NMR (100 MHz, CDCl3) δ (d, J = Hz), 134.5, 132.6, (d, J = 10.4 Hz), (q, J = Hz), (d, J = 9.6 Hz), (d, J = 26.6 Hz), (d, J = 24.7 Hz), 95.8 (d, J = 2.0 Hz); 19 F NMR (376 MHz, CDCl3) δ , Chloro-3-((trifluoromethyl)thio)-1H-indole (3l) 3 was obtained in 75% yield (75.5 mg) as a S-5
6 yellow oil. 1 H NMR (400 MHz, CDCl3) δ 8.46 (s, br, 1H), 7.74 (d, J = 1.2 Hz, 1H), 7.46 (d, J = 2.8 Hz, 1H), 7.25 (d, J = 8.4 Hz, 1H), 7.19 (dd, J = 8.4, 2.0 Hz, 1H); 13 C NMR (100 MHz, CDCl3) δ 134.4, 134.2, 130.7, (q, J = Hz), 127.7, 124.0, 118.9, 113.0, 95.4 (q, J = 2.4 Hz); 19 F NMR (376 MHz, CDCl3) δ Bromo-3-((trifluoromethyl)thio)-1H-indole (3m) 2 was obtained in 61% yield (72.2 mg) as a yellow oil. 1 H NMR (400 MHz, CDCl3) δ 8.52 (s, br, 1H), 7.91 (s, 1H), 7.48 (d, J = 2.4 Hz, 1H), 7.34 (d, J = 8.4 Hz, 1H), (m, 1H); 13 C NMR (100 MHz, CDCl3) δ 134.8, 133.9, 131.3, (q, J = Hz), 126.6, 122.0, 115.3, 113.3, 95.4 (q, J = 2.4 Hz); 19 F NMR (376 MHz, CDCl3) δ Methyl 3-((trifluoromethyl)thio)-1H-indole-5-carboxylate (3n) 4 was obtained in 58% yield (63.8 mg) as a yellow oil. 1 H NMR (400 MHz, acetone-d6) δ (s, br, 1H), 8.46 (s, 1H), 7.99 (d, J = 2.8 Hz, 1H), 7.94 (dd, J = 8.8, 1.6 Hz, 1H), (m, 1H), 3.92 (s, 3H); 13 C NMR (100 MHz, Acetone-d6) δ 167.8, 140.2, 137.2, (q, J = Hz), 130.0, 124.8, 124.3, 121.8, 113.3, (q, J = 2.4 Hz), 52.2; 19 F NMR (376 MHz, acetone-d6) δ Methyl-3-((trifluoromethyl)thio)-1H-indole (3o) was obtained in 75% yield (68.9 mg) as a yellow oil. 1 H NMR (400 MHz, CDCl3) δ 8.30 (s, 1H), 7.67 (d, J = 8.4 Hz, 1H), (m, 1H), 7.18 (s, 1H), 7.11 (d, J = 8.0 Hz, 1H), 2.47 (s, 3H); 13 C NMR (100 MHz, CDCl3) δ 136.6, 133.6, 132.3, (q, J = Hz), 127.4, 123.6, 119.1, 111.7, 95.4, 21.8; 19 F NMR (376 MHz, CDCl3) δ ; HRMS (ESI) calcd for C10H9F3NS + (M + H) , found Methoxy-3-((trifluoromethyl)thio)-1H-indole (3p) 3 was obtained in 63% yield (62.5 mg) as a S-6
7 yellow oil. 1 H NMR (400 MHz, CDCl3) δ 8.39 (s, 1H), 7.66 (d, J = 8.8 Hz, 1H), 7.43 (d, J = 2.4 Hz, 1H), 6.94 (dd, J = 8.8, 2.0 Hz, 1H), 6.89 (d, J = 2.0 Hz, 1H), 3.86 (s, 3H); 13 C NMR (100 MHz, CDCl3) δ 157.5, 137.0, 131.7, (q, J = Hz), 123.7, 120.2, 111.8, 95.7, 95.1, 55.8; 19 F NMR (376 MHz, CDCl3) δ Fluoro-3-((trifluoromethyl)thio)-1H-indole (3q) 2 was obtained in 52% yield (48.8 mg) as a yellow oil. 1 H NMR (400 MHz, CDCl3) δ 8.46 (s, br, 1H), 7.70 (dd, J = 8.4, 5.2 Hz, 1H), 7.49 (d, J = 2.4 Hz, 1H), (m, 2H); 13 C NMR (100 MHz, CDCl3) δ (d, J = Hz), (d, J = 12.6 Hz), 133.3, (q, J = Hz), 126.0, (d, J = 10.1 Hz), (d, J = 24.7 Hz), 98.2 (d, J = 26.6 Hz), 96.0 (q, J = 2.2 Hz); 19 F NMR (376 MHz, CDCl3) δ , Chloro-3-((trifluoromethyl)thio)-1H-indole (3r) 3 was obtained in 70% yield (70.4 mg) as a yellow oil. 1 H NMR (400 MHz, CDCl3) δ 8.42 (s, br, 1H), 7.68 (d, J = 8.8 Hz, 1H), 7.46 (d, J = 2.8 Hz, 1H), 7.34 (d, J = 1.2 Hz, 1H), 7.22 (dd, J = 8.8, 1.2 Hz, 1H); 13 C NMR (100 MHz, CDCl3) δ 136.4, 133.5, 129.5, (q, J = Hz), 128.1, 122.6, 120.4, 111.8, 96.1 (q, J = 2.5 Hz); 19 F NMR (376 MHz, CDCl3) δ Bromo-3-((trifluoromethyl)thio)-1H-indole (3s) was obtained in 52% yield (61.4 mg) as a yellow oil. 1 H NMR (400 MHz, CDCl3) δ 8.39 (s, br, 1H), 7.62 (d, J = 8.4 Hz, 1H), 7.47 (s, 1H), 7.43 (d, J = 1.2 Hz, 1H), 7.34 (d, J = 8.4 Hz, 1H); 13 C NMR (100 MHz, CDCl3) δ 136.8, 133.4, (q, J = Hz), 128.4, 125.1, 120.8, 117.1, 114.7, 96.1 (q, J = 2.4 Hz); 19 F NMR (376 MHz, CDCl3) δ ; HRMS (ESI) calcd for C9H6BrF3NS + (M + H) , found ,6-Difluoro-3-((trifluoromethyl)thio)-1H-indole (3t) was obtained in 45% yield (45.6 mg) as a S-7
8 yellow oil. 1 H NMR (400 MHz, CDCl3) δ 8.59 (s, 1H), (m, 2H), 7.22 (dd, J = 10.0, 6.4 Hz, 1H); 13 C NMR (100 MHz, CDCl3) δ (dd, J = 243.6, 16.0 Hz), (dd, J = 241.2, 14.8 Hz), 134.2, (d, J = 10.7 Hz), (q, J = Hz), (d, J = 8.1 Hz), (d, J = 20.2 Hz), (d, J = 22.3 Hz), 96.2; 19 F NMR (376 MHz, CDCl3) δ , (d, J = 20.6 Hz), (d, J = 20.6 Hz); HRMS (ESI) calcd for C9H5F5NS + (M + H) , found Methyl-3-((trifluoromethyl)thio)-1H-indole (3u) 2 was obtained in 78% yield (72.5 mg) as a yellow oil. 1 H NMR (400 MHz, CDCl3) δ 8.20 (s, br, 1H), 7.64 (d, J = 8.0 Hz, 1H), 7.35 (d, J = 2.8 Hz, 1H), 7.17 (t, J = 7.6 Hz, 1H), 7.04 (d, J = 7.2 Hz, 1H), 2.37 (s, 3H); 13 C NMR (100 MHz, CDCl3) δ 135.7, 132.7, (q, J = Hz), 129.2, 124.0, 121.9, 121.1, 117.0, 95.9 (dd, J = 2.4 Hz), 16.2; 19 F NMR (376 MHz, CDCl3) δ Methoxy-3-((trifluoromethyl)thio)-1H-indole (3v) 5 was obtained in 85% yield (84.3 mg) as a yellow oil. 1 H NMR (400 MHz, CDCl3) δ 8.71 (s, br, 1H), (m, 2H), 7.18 (dd, J = 10.4, 8.0 Hz, 1H), 6.70 (d, J = 7.6 Hz, 1H), 3.93 (s, 3H); 13 C NMR (100 MHz, CDCl3) δ 146.4, 132.4, 130.9, (q, J = Hz), 126.8, 122.2, 111.8, 103.2, 95.8 (d, J = 2.4 Hz), 55.6; 19 F NMR (376 MHz, CDCl3) δ Methyl-3-((trifluoromethyl)thio)-1H-indole (3w) 2 was obtained in 46% yield (42.5 mg) as a yellow oil. 1 H NMR (400 MHz, CDCl3) δ 8.19 (s, br, 1H), 7.70 (d, J = 7.2 Hz, 1H), (m, 3H), 2.51 (s, 3H); 13 C NMR (100 MHz, CDCl3) δ 143.7, 135.1, 130.7, (q, J = Hz), 122.7, 121.5, 118.8, 110.9, 92.6 (q, J = 2.2 Hz), 12.1; 19 F NMR (376 MHz, CDCl3) δ S-8
9 5-Methoxy-2-methyl-3-((trifluoromethyl)thio)-1H-indole (3x) 6 was obtained in 52% yield (54.1 mg) as a yellow oil. 1 H NMR (400 MHz, CDCl3) δ 8.26 (s, br, 1H), (m, 2H), 6.84 (dd, J = 8.8, 2.4 Hz, 1H), 3.88 (s, 3H), 2.52 (s, 3H); 13 C NMR (100 MHz, CDCl3) δ 155.5, 144.2, 131.6, (q, J = Hz), 129.9, 112.6, 111.7, 100.6, 92.2, 56.0, 12.3; 19 F NMR (376 MHz, CDCl3) δ Fluoro-2-methyl-3-((trifluoromethyl)thio)-1H-indole (3y) was obtained in 69% yield (68.6 mg) as a yellow oil. 1 H NMR (400 MHz, CDCl3) δ 8.32 (s, br, 1H), 7.34 (dd, J = 8.8, 1.6 Hz, 1H), 7.20 (dd, J = 8.8, 4.0 Hz, 1H), 6.93 (td, J = 11.2, 2.4 Hz, 1H), 2.54 (s, 3H); 13 C NMR (100 MHz, CDCl3) δ (d, J = Hz), 145.5, (d, J = 10.3 Hz), 131.5, (q, J = Hz), (d, J = 9.6 Hz), (d, J = 26.3 Hz), (d, J = 24.7 Hz), 92.9 (q, J = 2.4 Hz), 12.3; 19 F NMR (376 MHz, CDCl3) δ , ; HRMS (ESI) calcd for C10H8F4NS + (M + H) , found ,6-Dimethyl-3-((trifluoromethyl)thio)-1H-indole (3z) was obtained in 43% yield (41.9 mg) as a yellow oil. 1 H NMR (400 MHz, CDCl3) δ 8.16 (s, br, 1H), 7.48 (s, 1H), 7.17 (d, J = 8.2 Hz, 1H), 7.02 (d, J = 8.2 Hz, 1H), 2.52 (s, 3H), 2.47 (s, 3H); 13 C NMR (100 MHz, CDCl3) δ 143.7, 133.4, 131.0, 130.9, (d, J = Hz), 124.2, 118.5, 110.6, 92.0 (d, J = 1.9 Hz), 21.6, 12.2; 19 F NMR (376 MHz, CDCl3) δ ; HRMS (ESI) calcd for C11H11F3NS + (M + H) , found Phenyl-3-((trifluoromethyl)thio)-1H-indole (3aa) 2 was obtained in 70% yield (82.0 mg) as a yellow oil. 1 H NMR (400 MHz, CDCl3) δ 8.40 (s, br, 1H), (m, 1H), (m, 2H), (m, 3H), (m, 1H), (m, 2H); 13 C NMR (100 MHz, CDCl3) δ 144.5, 135.4, 131.5, 130.7, (q, J = Hz), 129.4, 128.9, 128.8, 123.8, 121.9, 119.9, 111.4, 92.4 (d, S-9
10 J = 2.3 Hz); 19 F NMR (376 MHz, CDCl3) δ Methyl-2-phenyl-3-((trifluoromethyl)thio)-1H-indole (3ab) 7 was obtained in 64% yield (78.8 mg) as a yellow oil. 1 H NMR (400 MHz, CDCl3) δ 7.85 (d, J = 7.2 Hz, 1H), (m, 3H), (m, 3H), (m, 2H), 3.63 (s, 3H); 13 C NMR (100 MHz, CDCl3) δ 148.2, 137.2, 130.9, 130.3, 129.9, (q, J = Hz), 129.3, 128.5, 123.3, 121.8, 119.7, 110.1, 92.7 (d, J = 2.2 Hz), 31.8; 19 F NMR (376 MHz, CDCl3) δ SCF 3 N Me 3ac 1-Methyl-3-((trifluoromethyl)thio)-1H-indole (3ac) 2 was obtained in 61% yield (56.4 mg) as a yellow oil. 1 H NMR (400 MHz, CDCl3) δ 7.78 (d, J = 7.6 Hz, 1H), (m, 4H), 3.77 (s, 3H); 13 C NMR (100 MHz, CDCl3) δ 137.3, 137.1, 130.3, (q, J = Hz), 123.0, 121.4, 119.5, 110.0, 93.1 (q, J = 2.4 Hz), 33.4; 19 F NMR (376 MHz, CDCl3) δ SCF 3 N Bn 3ad 1-Benzyl-3-((trifluoromethyl)thio)-1H-indole (3ad) 8 was obtained in 69% yield (84.7 mg) as a yellow oil. 1 H NMR (400 MHz, CDCl3) δ (m, 1H), 7.38 (s, 1H), (m, 6H), (m, 2H), 5.22 (s, 2H); 13 C NMR (100 MHz, CDCl3) δ 136.9, 136.5, 136.2, 130.5, (q, J = Hz), 129.1, 128.2, 127.1, 123.2, 121.6, 119.7, 110.6, 94.0 (q, J = 2.3 Hz), 50.6; 19 F NMR (376 MHz, CDCl3) δ Sulfenylation of pyrole 5 with TfNHNHBoc (eqn (1)) The procedure for the sulfenylation of pyrole 5 with TfNHNHBoc is the same as that for the sulfenylation of indoles (see above). N SCF 3 Bn 5 1-Benzyl-2-((trifluoromethyl)thio)-1H-pyrrole (5) 9 was obtained in 30% yield (30.5 mg) as a S-10
11 yellow oil. 1 H NMR (400 MHz, CDCl3) δ (m, 3H), (m, 2H), 6.91 (s, 1H), 6.72 (s, 1H), 6.26 (d, J = 2.8 Hz, 1H), 5.25 (s, 2H); 13 C NMR (100 MHz, CDCl3) δ 137.5, 128.9, (q, J = Hz), 127.9, 127.6, 127.2, 123.1, 109.9, (q, J = 2.3 Hz), 50.7; 19 F NMR (376 MHz, CDCl3) δ Mechanistic studies eqn (2) To a reaction tube equipped with a magnetic stir bar was charged with TfNHNHBoc (2a) (211 mg, 0.80 mmol). The tube was sealed with a septum, evacuated, and backfilled with nitrogen three times. Acetonitrile (2.0 ml) was added via syringe with gentle stirring. The reaction vessel was allowed to stir at 80 C for 4 h. A small portion of the mixture was subjected to 19 F NMR spectroscopic analysis (using PhCF3 as an internal standard), and CF3SSCF3 was identified. CF3SSCF3: 19 F NMR (376 MHz, CDCl3) δ eqn (3) S-11
12 To a reaction tube equipped with a magnetic stir bar was charged with TfNHNHBoc (2a) (211 mg, 0.80 mmol) and CuCl (79.2 mg, 0.80 mmol). The tube was sealed with a septum, evacuated, and backfilled with nitrogen three times. Acetonitrile (2.0 ml) was added via syringe with gentle stirring. The reaction vessel was allowed to stir at 80 C for 0.5 h. A small portion of the mixture was subjected to 19 F NMR spectroscopic analysis (using PhCF3 as an internal standard), and CuSCF3 was identified. CuSCF3: 19 F NMR (376 MHz, CDCl3) δ eqn (4) To a reaction tube equipped with a magnetic stir bar was charged with TfNHNHBoc (2a) (211 mg, 0.80 mmol). The tube was sealed with a septum, evacuated, and backfilled with nitrogen three times. Acetonitrile (2.0 ml) was added via syringe with gentle stirring. After stir at 80 C for 4 h, indole (1a) (46.9 mg, 0.40 mmol), CuCl (4.0 mg, 10 mol%), and DMSO (31.2 mg, 28 μl, 0.40 mmol) was added to the reaction tube. The mixture was stirred at 80 C for 10 h to give thioether 3a in 25% yield (determined by 19 F NMR spectroscopic analysis using PhCF3 as an internal standard). S-12
13 eqn (5) To a reaction tube equipped with a magnetic stir bar was charged with TfNHNHBoc (2a) (211 mg, 0.80 mmol) and indole (1a) (46.9 mg, 0.40 mmol). The tube was sealed with a septum, evacuated, and backfilled with nitrogen three times. DMSO (31.2 mg, 28 μl, 0.4 mmol) and MeCN (2.0 ml) were added via syringe with gentle stirring. The reaction vessel was allowed to stir at 80 C for 10 h. Only a trace amount of thioether 3a was determined by 19 F NMR spectroscopic analysis. S-13
14 eqn (6) To a reaction tube equipped with a magnetic stir bar was charged with TfNHNHBoc (2a) (211 mg, 0.80 mmol), indole (1a) (46.9 mg, 0.40 mmol), dibenzyl sulfoxide (92.1 mg, 0.40 mmol), and CuCl (4.0 mg, 10 mol%). The tube was sealed with a septum, evacuated, and backfilled with nitrogen three times. MeCN (2.0 ml) was added via syringe with gentle stirring. The reaction vessel was allowed to stir at 80 C for 10 h. The mixture was cooled to room temperature and purified directly by silica gel chromatography, eluting with ethyl acetate/petroleum ether (1:10), to give thioether 3a in 61% yield (52.9 mg) and BnSBn in 41% yield (35.0 mg). BnSBn: 1 H NMR (400 MHz, CDCl3) δ (m, 10H), 3.59 (s, 4H); 13 C NMR (100 MHz, CDCl3) δ 138.2, 129.1, 128.6, 127.1, References 1 J.-Y. Guo, R.-X. Wu, J.-K. Jin and S.-K. Tian, Org. Lett., 2016, 18, H. Chachignon, M. Maeno, H. Kondo, N. Shibata and D. Cahard, Org. Lett., 2016, 18, S-14
15 3 X. Zhao, A. Wei, B. Yang, T. Li, Q. Li, D. Qiu and K. Lu, J. Org. Chem., 2017, 82, L. Jiang, J. Qian, W. Yi, G. Lu, C. Cai and W. Zhang, Angew. Chem. Int. Ed., 2015, 54, D.-W. Sun, X. Jiang, M. Jiang, Y. Lin and J.-T. Liu, Eur. J. Org. Chem., 2017, P. Zhang, M. Li, X.-S. Xue, C. Xu, Q. Zhao, Y. Liu, H. Wang, Y. Guo, L. Lu and Q. Shen, J. Org. Chem., 2016, 81, J. Sheng, S. Li and J. Wu, Chem. Commun., 2014, 50, M.-j. Bu, G.-p. Lu and C. Cai, Org. Chem. Front., 2017, 4, Z. Huang, Y.-D. Yang, E. Tokunaga and N. Shibata, Org. Lett., 2015, 17, Y. Yang, L. Xu, S. Yu, X. Liu, Y. Zhang and D. A. Vicic, Chem. Eur. J., 2016, 22, S. Enthaler and M. Weidauer, Catal. Lett., 2011, 141, 833. S-15
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