Copper-catalyzed formal O-H insertion reaction of α-diazo-1,3-dicarb- onyl compounds to carboxylic acids with the assistance of isocyanide

Σχετικά έγγραφα
A facile and general route to 3-((trifluoromethyl)thio)benzofurans and 3-((trifluoromethyl)thio)benzothiophenes

Supporting Information for

Supporting Information for. Catalytic C H α-trifluoromethylation of α,β-unsaturated Carbonyl Compounds

Copper-Catalyzed Oxidative Dehydrogenative N-N Bond. Formation for the Synthesis of N,N -Diarylindazol-3-ones

Supporting Information for: Intramolecular Hydrogen Bonding-Assisted Cyclocondensation of. 1,2,3-Triazole Synthesis

Supporting Information

Enantioselective Organocatalytic Michael Addition of Isorhodanines. to α, β-unsaturated Aldehydes

Highly enantioselective cascade synthesis of spiropyrazolones. Supporting Information. NMR spectra and HPLC traces

Divergent synthesis of various iminocyclitols from D-ribose

Supporting Information

Supporting Information

Supporting Information

Direct Palladium-Catalyzed Arylations of Aryl Bromides. with 2/9-Substituted Pyrimido[5,4-b]indolizines

Free Radical Initiated Coupling Reaction of Alcohols and. Alkynes: not C-O but C-C Bond Formation. Context. General information 2. Typical procedure 2

and Selective Allylic Reduction of Allylic Alcohols and Their Derivatives with Benzyl Alcohol

Supporting information

Supporting Information

Metal-free Oxidative Coupling of Amines with Sodium Sulfinates: A Mild Access to Sulfonamides

Electronic Supplementary Information

Supporting Information. Asymmetric Binary-acid Catalysis with Chiral. Phosphoric Acid and MgF 2 : Catalytic

First DMAP-mediated direct conversion of Morita Baylis. Hillman alcohols into γ-ketoallylphosphonates: Synthesis of

Supporting Information

Site-Selective Suzuki-Miyaura Cross-Coupling Reactions of 2,3,4,5-Tetrabromofuran

9-amino-(9-deoxy)cinchona alkaloids-derived novel chiral phase-transfer catalysts

Supporting Information

Fluorinative Ring-opening of Cyclopropanes by Hypervalent Iodine Reagents. An Efficient Method for 1,3- Oxyfluorination and 1,3-Difluorination

Supporting Information. Experimental section

Supporting information

Regioselectivity in the Stille coupling reactions of 3,5- dibromo-2-pyrone.

Vilsmeier Haack reagent-promoted formyloxylation of α-chloro-narylacetamides

Supporting Information

Room Temperature Highly Diastereoselective Zn-Mediated. Allylation of Chiral N-tert-Butanesulfinyl Imines: Remarkable Reaction Condition Controlled

Facile construction of the functionalized 4H-chromene via tandem. benzylation and cyclization. Jinmin Fan and Zhiyong Wang*

Hiyama Cross-Coupling of Chloro-, Fluoroand Methoxy- pyridyl trimethylsilanes : Room-temperature Novel Access to Functional Bi(het)aryl

Supporting Information. Copyright Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim, 2006

Direct Transformation of Ethylarenes into Primary Aromatic Amides with N-Bromosuccinimide and I 2 -aq NH 3

Phosphorus Oxychloride as an Efficient Coupling Reagent for the Synthesis of Ester, Amide and Peptide under Mild Conditions

gem-dichloroalkenes for the Construction of 3-Arylchromones

Aminofluorination of Fluorinated Alkenes

Synthesis of novel 1,2,3-triazolyl derivatives of pregnane, androstane and D-homoandrostane. Tandem Click reaction/cu-catalyzed D-homo rearrangement

Supporting Information

Supplementary Data. Engineering, Nanjing University, Nanjing , P. R. China;

Selective mono reduction of bisphosphine

Supplementary information

ESI for. A simple and efficient protocol for the palladium-catalyzed. ligand-free Suzuki reaction at room temperature in aqueous DMF.

Oxyhalogenation of thiols and disulfides into sulfonyl chlorides/ bromides in water using oxone-kx(x= Cl or Br)

Catalyst-free transformation of levulinic acid into pyrrolidinones with formic acid

Supporting Information. Experimental section

Synthesis and evaluation of novel aza-caged Garcinia xanthones

Copper-Catalyzed Direct Acyloxylation of C(sp 2 ) H Bonds. in Aromatic Amides

Iodine-catalyzed synthesis of sulfur-bridged enaminones and chromones via double C(sp 2 )-H thiolation

Supporting Information

Eco-friendly synthesis of diverse and valuable 2-pyridones by catalyst- and solvent-free thermal multicomponent domino reaction

Copper-Catalyzed Oxidative Coupling of Acids with Alkanes Involving Dehydrogenation: Facile Access to Allylic Esters and Alkylalkenes

The Free Internet Journal for Organic Chemistry

Supporting Information

Supporting Information

Supplementary Material

Supporting Information One-Pot Approach to Chiral Chromenes via Enantioselective Organocatalytic Domino Oxa-Michael-Aldol Reaction

Copper-mediated radical cross-coupling reaction of 2,2-dichloro-1,1,1-trifluoroethane (HCFC-123) with phenols or thiophenols. Support Information

Kishore Natte, Jianbin Chen, Helfried Neumann, Matthias Beller, and Xiao-Feng Wu*

Rhodium-Catalyzed Oxidative Decarbonylative Heck-type Coupling of Aromatic Aldehydes with Terminal Alkenes

Supporting Information

Tributylphosphine-Catalyzed Cycloaddition of Aziridines with Carbon Disulfide and Isothiocyanate

Supporting Information

Novel and Selective Palladium-Catalyzed Annulation of 2-Alkynylphenols to Form 2-Substituted 3-Halobenzo[b]furans. Supporting Information

Peptidomimetics as Protein Arginine Deiminase 4 (PAD4) Inhibitors

Supporting Information. Consecutive hydrazino-ugi-azide reactions: synthesis of acylhydrazines bearing 1,5- disubstituted tetrazoles

Supporting Information for Iron-catalyzed decarboxylative alkenylation of cycloalkanes with arylvinylic carboxylic acids via a radical process

Supporting Information

Electronic Supplementary Information

Chiral Brønsted Acid Catalyzed Enantioselective Intermolecular Allylic Aminations. Minyang Zhuang and Haifeng Du*

Lewis Acid Catalyzed Propargylation of Arenes with O-Propargyl Trichloroacetimidate: Synthesis of 1,3-Diarylpropynes

Supporting Information

The N,S-Bidentate Ligand Assisted Pd-Catalyzed C(sp 2 )-H. Carbonylation using Langlois Reagent as CO Source. Supporting Information.

Rh(III)-Catalyzed C-H Amidation with N-hydroxycarbamates: A. new Entry to N-Carbamate Protected Arylamines

Cu-Catalyzed/Mediated Synthesis of N-Fluoroalkylanilines from Arylboronic Acids: Fluorine Effect on the Reactivity of Fluoroalkylamines

multicomponent synthesis of 5-amino-4-

Supporting Information. Synthesis and biological evaluation of nojirimycin- and

Supporting Information. Synthesis and biological evaluation of 2,3-Bis(het)aryl-4-azaindoles Derivatives as protein kinases inhibitors

Aluminium-mediated Aromatic C F Bond Activation: Regioswitchable Construction of Benzene-fused Triphenylene. Frameworks

Supporting Information. Copyright Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim, 2007

Supporting Information. Table of Contents. II. Experimental procedures. II. Copies of 1H and 13C NMR spectra for all compounds

Supporting Information for Synthesis of Fused N-Heterocycles via Tandem C-H Activation

Supporting Information. for. Highly Selective Hydroiodation of Alkynes Using. Iodine-Hydrophosphine Binary System

Supporting Information for. Copper-Catalyzed Radical Reaction of N-Tosylhydrazones: Stereoselective Synthesis of (E)-Vinyl Sulfones

Copper-promoted hydration and annulation of 2-fluorophenylacetylene derivatives: from alkynes to benzo[b]furans and benzo[b]thiophenes

Pd Catalyzed Carbonylation for the Construction of Tertiary and

Supporting Information

Electronic Supplementary Information (ESI)

Supporting Information

Supporting Information for

Supporting information

Supplement: Intramolecular N to N acyl migration in conformationally mobile 1 -acyl-1- systems promoted by debenzylation conditions (HCOONH 4

Supporting Information for

Supporting Information

Supplementary Figure S1. Single X-ray structure 3a at probability ellipsoids of 20%.

Supplementary Information for

Supporting Information

Supporting Information. Microwave-assisted construction of triazole-linked amino acid - glucoside conjugates as novel PTP1B inhibitors

Transcript:

Electronic Supplementary Material (ESI) for ChemComm. This journal is The Royal Society of Chemistry 2014 Copper-catalyzed formal O-H insertion reaction of α-diazo-1,3-dicarb- onyl compounds to carboxylic acids with the assistance of isocyanide Zikun Wang, a Xihe Bi, b Yongjiu Liang, a * Peiqiu Liao, b Dewen Dong a * a Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun 130022, China. b Department of Chemistry, Northeast Normal University, Changchun 130024, China. E-mail: yjliang@ciac.ac.cn; dwdong@ciac.ac.cn Electronic Supplementary Information Contents I. General information... S2 II. Synthesis and analytical data of 3... S2-S7 III. NMR spectra copies... S8-25 S1

I. General information All reagents were purchased from commercial sources and used without treatment, unless otherwise indicated. The products were purified by column chromatography over silica gel. 1 H-NMR and 13 C-NMR spectra were recorded at 25 ºC on a Varian 300 MHz or 400 MHz and 100 MHz spectrometer, respectively, and TMS was used as internal standard. Mass spectra were recorded on BRUKER AutoflexIII Smartbeam MS-spectrometer. High resolution mass spectra (HRMS) were recorded on Bruck microtof by using ESI method. II. Synthesis and analytical data of compounds 3 O O O O CO O 2 Et C N R 2 R 1 R 1 R 2 + R 3 OH R 3 O N Cu(OAc) 2,100 o C 2 O 1 2 3 Typical synthetic procedure (with 3a as an example): To a solution of α-diazo-β-oxoamide (1a) (1.0 mmol) and ethyl isocyanoacetate (0.5 mmol) in acetic acid (4.0 ml) was added Cu(OAc) 2 (0.1 mmol) in one portion at 100 o C under sirring. After being stirred for 5 hours, the reaction mixture was cooled to room temperature and saturated aqueous NaCl solution (20 ml) was added under stirring. The mixture was extracted with dichloromethane (3 20 ml) and the combined organic phase was washed with water (3 20mL), dried over MgSO 4, filtered, and concentrated under vacuum. Purification of the crude product by flash column chromatography (silica gel; petroleum ether: ethyl acetate = 8 : 1) gave 3a in 83% yield as a white solid. (3a) White solid, m.p. 66-68 o C; 1 H-NMR (300 MHz, CDCl 3 ) δ 2.25 (s, 3H), 2.44 (s, 3H), 5.62 (s, 1H), 7.13 (t, J = 7.2 Hz, 1H), 7.31 (t, J = 7.8 Hz, 2H), 7.50 (d, J = 7.8 Hz, 2H), 8.26 (s, 1H) ; 13 C-NMR (CDCl 3, 100 MHz) δ 20.28, 27.46, 79.06, 120.12, 125.07, 128.91, 136.37, 161.08, 168.60, 199.86; HRMS (ESI) m/z calculated for C 12 H 13 NO 4 [M+Na] + : 258.0740 found: 258.0742. (3b) Yellowish solid, m.p. 43-45 o C; 1 H-NMR (300 MHz, CDCl 3 ) δ 2.23 (s, 3H), 2.26 (s, 3H), 2.40 (s, 3H), 5.56 (s, 1H), 7.08 (d, J = 8.1 Hz, 2H), 7.32 (d, J = 8.1 Hz, 2H), 7.90 (s, 1H) ; 13 C-NMR (CDCl 3, 100 S2

MHz) δ 20.40, 20.76, 27.60, 79.13, 120.20, 129.48, 133.80, 134.88, 160.87, 168.54, 199.82; HRMS (ESI) m/z calculated for C 13 H 15 NO 4 [M+Na] + : 272.0903 found: 272.0899. (3c) White solid, m.p. 68-70 o C; 1 H-NMR (300 MHz, CDCl 3 ) δ 2.27 (s, 3H), 2.31 (s, 3H), 5.67 (s, 1H), 7.11 (t, J = 7.5 Hz, 1H), 7.21 (d, J = 7.5 Hz, 2H), 7.81 (d, J = 7.8 Hz, 1H), 8.03 (s, 1H); 13 C-NMR (CDCl 3, 100 MHz) δ 17.35, 20.42, 27.67, 79.19, 122.69, 125.83, 126.80, 129.21, 130.55, 134.27, 161.00, 168.51, 200.09; HRMS (ESI) m/z calculated for C 13 H 15 NO 4 [M+Na] + : 272.0905 found: 272.0899. (3d) Yellowish solid, m.p. 66-67 o C; 1 H-NMR (400 MHz, CDCl 3 ) δ 2.26 (s, 3H), 2.44 (s, 3H), 5.61 (s, 1H), 7.28 (d, J = 8.4 Hz, 2H), 7.46 (d, J = 8.4 Hz, 2H), 8.24 (s, 1H) ; 13 C-NMR (CDCl 3, 100 MHz) δ 20.36, 27.58, 78.99, 121.40, 129.03, 130.20, 135.00, 161.07, 168.54, 199.98; HRMS (ESI) m/z calculated for C 12 H 12 ClNO 4 [M+Na] + : 292.0338 found: 292.0353. O O O N H Cl O (3e) White solid, m.p. 77-79 o C; 1 H-NMR (300 MHz, CDCl 3 ) δ 2.32 (s, 3H), 2.49 (s, 3H), 5.68 (s, 1H), 7.07-7.13 (m, 1H), 7.29-7.32 (m, 1H), 7.38-7.41 (m, 1H), 8.76 (s, 1H) ; 13 C-NMR (CDCl 3, 100 MHz) δ 20.36, 27.68, 79.03, 121.42, 123.32, 125.51, 127.75, 129.15, 133.33, 161.07, 168.32, 198.99; HRMS (ESI) m/z calculated for C 12 H 12 ClNO 4 [M+Na] + : 292.0348 found: 292.0353. S3

(3f) White solid, m.p. 74-75 o C; 1 H-NMR (400 MHz, CDCl 3 ) δ 2.27 (s, 3H), 2.44 (s, 3H), 5.62 (s, 1H), 7.56 (d, J = 8.0 Hz, 2H), 7.63 (d, J = 8.0 Hz, 2H), 8.34 (s, 1H) ; 13 C-NMR (CDCl 3, 100 MHz) δ 20.40, 27.62, 79.00, 119.83, 123.86 (q, 1 J CF = 270.0 Hz), 126.31, 126.98 (q, 2 J CF = 32.9 Hz), 139.53, 161.33, 168.58, 200.12; HRMS (ESI) m/z calculated for C 13 H 12 F 3 NO 4 [M+Na] + : 326.0621 found: 326.0616. (3g) Yellow solid, m.p. 71-74 o C; 1 H-NMR (300 MHz, CDCl 3 ) δ 2.21 (s, 3H), 2.28 (s, 6H), 2.45 (s, 3H), 5.64 (s, 1H), 7.01 (s, 2H), 7.57-7.60 (m, 1H), 7.97 (s, 1H) ; 13 C-NMR (CDCl 3, 100 MHz) δ 17.27, 20.37, 20.75, 27.61, 79.18, 123.00, 127.24, 129.58, 131.17, 131.55, 135.65, 161.03, 168.50, 199.98; HRMS (ESI) m/z calculated for C 14 H 17 NO 4 [M+Na] + : 286.1057 found: 286.1055. (3h) Yellow-oil liquid; 1 H-NMR (300 MHz, CDCl 3 ) δ 0.92 (t, J = 7.5 Hz, 3H), 1.58-1.70 (m, 2H), 2.25 (s, 3H), 2.67-2.92 (m, 2H), 5.60 (s, 1H), 7.14 (t, J = 7.5 Hz, 1H), 7.30 (t, J = 7.5 Hz, 2H), 7.51 (d, J = 7.8 Hz, 2H), 8.18 (s, 1H) ; 13 C-NMR (CDCl 3, 100 MHz) δ 13.26, 16.33, 20.32, 41.89, 78.89, 120.11, 125.04, 128.92, 136.42, 161.19, 168.56, 202.16; HRMS (ESI) m/z calculated for C 14 H 17 NO 4 [M+Na] + : 286.1048 found: 286.1055. O O Ph O NHPh O S4

(3i) Yellow solid, m.p. 126-128 o C; 1 H-NMR (300 MHz, CDCl 3 ) δ 2.29 (s, 3H), 6.45 (s, 1H), 7.13 (t, J = 7.5 Hz, 1H), 7.31 (t, J = 7.5 Hz, 2H), 7.48-7.53 (m, 4H), 7.63 (t, J = 7.5 Hz, 1H), 8.11 (s, 1H), 8.18 (d, J = 7.5 Hz, 2H); 13 C-NMR (CDCl 3, 100 MHz) δ 20.49, 76.51, 120.08, 125.12, 128.63, 128.98, 129.71, 134.17, 134.30, 136.49, 161.47, 168.59, 191.59; HRMS (ESI) m/z calculated for C 17 H 15 NO 4 [M+Na] + : 320.0891 found: 320.0899. (3j) Yellow-oil liquid; 1 H-NMR (300 MHz, CDCl 3 ) δ 1.24 (t, J = 7.2 Hz, 3H), 2.15 (s, 3H), 2.27 (s, 3H), 4.21 (q, J = 7.2 Hz, J = 14.4 Hz, 2H), 5.42 (s, 1H) ; 13 C-NMR (CDCl 3, 100 MHz) δ 13.65, 20.02, 26.82, 62.14, 77.62, 164.25, 169.14, 197.27; HRMS (ESI) m/z calculated for C 8 H 12 O 5 [M+Na] + : 211.0586 found: 211.0582. (3k) Yellow-oil liquid; 1 H-NMR (300 MHz, CDCl 3 ) δ 1.21 (t, J = 7.2 Hz, 3H), 2.23 (s, 3H), 4.24 (q, J = 7.2 Hz, J = 14.4 Hz, 2H), 6.32 (s, 1H), 7.50 (t, J = 7.5 Hz, 2H), 7.63 (t, J = 7.5 Hz, 1H), 7.99 (d, J = 7.5 Hz, 2H); 13 C-NMR (CDCl 3, 100 MHz) δ 13.72, 20.30, 62.30, 74.37, 128.31, 128.64, 129.03, 134.06, 165.01, 169.35, 189.55; HRMS (ESI) m/z calculated for C 13 H 14 O 5 [M+Na] + : 273.0731 found: 273.0739. (3l) Yellow-oil liquid; 1 H-NMR (300 MHz, CDCl 3 ) δ 2.23 (s, 3H), 2.29 (s, 3H), 6.26 (s, 1H), 7.48 (t, J = 7.5Hz, 2H), 7.62 (t, J = 7.5 Hz, 1H), 8.00 (d, J = 7.5 Hz, 2H); 13 C-NMR (CDCl 3, 100 MHz) δ 20.47, 26.79, 82.15, 128.72, 129.42, 131.52, 134.22, 169.24, 190.84, 199.40; HRMS (ESI) m/z calculated for C 12 H 12 O 4 [M+Na] + : 243.0622 found: 243.0633. S5

(3m) White solid, m.p. 62-64 o C; 1 H-NMR (300 MHz, CDCl 3 ) δ 2.44 (s, 3H), 3.89 (d, J = 2.1 Hz, 2H), 5.63 (s, 1H), 7.12-7.16 (m, 1H), 7.28-7.43 (m, 9H), 7.70 (s, 1H); 13 C-NMR (CDCl 3, 100 MHz) δ 27.72, 40.81, 79.08, 119.95, 125.14, 127.59, 128.90, 129.01, 129.38, 133.01, 136.34, 160.82, 168.88,199.14; HRMS (ESI) m/z calculated for C 18 H 17 NO 4 [M+Na] + : 334.1049 found: 334.1055. (3n) Yellow-oil liquid; 1 H-NMR (400 MHz, CDCl 3 ) δ 1.00-1.10 (m, 4H), 1.82-1.83 (m, 1H), 2.43 (s, 3H), 5.63 (s, 1H), 7.15 (t, J = 7.8 Hz, 1H), 7.32 (t, J = 7.8 Hz, 2H), 7.51 (d, J = 7.8 Hz, 2H), 8.30 (s, 1H) ; 13 C-NMR (CDCl 3, 100 MHz) δ 9.38, 9.51, 12.42, 27.54, 78.94, 120.16, 125.07, 128.94, 136.45, 161.23, 172.77, 200.13; HRMS (ESI) m/z calculated for C 14 H 15 NO 4 [M+Na] + : 284.0899 found: 284.0899. (3o) Red-oil liquid; 1 H-NMR (400 MHz, CDCl 3 ) δ 2.48 (s, 3H), 5.71 (s, 1H), 6.03 (d, J = 10.4 Hz, 1H), 6.30-6.36 (m, 1H), 6.59 (d, J = 17.2 Hz, 1H), 7.16 (t, J = 7.2 Hz, 1H), 7.34 (t, J = 7.6 Hz, 2H), 7.51 (d, J = 7.6 Hz, 2H), 8.12 (s, 1H) ; 13 C-NMR (CDCl 3, 100 MHz) δ 27.64, 79.06, 120.20, 125.20, 126.46, 129.04, 133.57, 136.41, 160.97, 163.78, 199.91; HRMS (ESI) m/z calculated for C 13 H 13 NO 4 [M+Na] + : 270.0733 found: 270.0742. (3p) Yellow-oil liquid; 1 H-NMR (300 MHz, CDCl 3 ) δ 2.46 (s, 3H), 3.50 (s, 3H), 4.28 (s, 2H), 5.72 (s, 1H), 7.15 (t, J = 7.5 Hz, 1H), 7.33 (t, J = 7.5 Hz, 2H), 7.50 (d, J = 8.1 Hz, 2H), 8.22 (s, 1H) ; 13 C-NMR S6

(CDCl 3, 100 MHz) δ 27.56, 59.52, 69.40, 79.07, 120.25, 125.28, 129.07, 136.36, 160.67, 168.26, 199.44; HRMS (ESI) m/z calculated for C 13 H 15 NO 5 [M+Na] + : 288.0841 found: 288.0848. Yellow-oil liquid; 1 H-NMR (400 MHz, CDCl 3 ) δ 1.15 (t, J = 7.2 Hz, 3H), 3.91 (d, J = 5.6 Hz, 2H), 4.07 (q, J = 7.2 Hz, 14.0 Hz, 2H), 7.08 (s, 1H), 8.10 (s, 1H) ; 13 C-NMR (CDCl 3, 100 MHz) δ 13.67, 39.53, 61.10, 161.58, 169.26; HRMS (ESI) m/z calculated for C 5 H 10 NO 3 [M+H] + : 132.0800 found: 132.0661. S7

Ⅲ. NMR spectra copies S8

S9

S10

S11

S12

S13

S14

S15

S16

S17

S18

S19

S20

S21

S22

S23

S24

S25