Cesium carbonate → N,N-Dimethyl-2-(5-thiophen-2-yl-1H-indol-3-yl)-acetamide

HRID 2427912ノート

反応式

HRID 2427912 の反応式
Br[C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][CH:10]=1)[NH:7][CH:6]=[C:5]2[CH2:11][C:12]([N:14]([CH3:16])[CH3:15])=[O:13].[S:17]1[CH:21]=[CH:20][CH:19]=[C:18]1B(O)O.C(=O)([O-])[O-].[Cs+].[Cs+].[OH-].[Na+]>COCCOC>[CH3:15][N:14]([CH3:16])[C:12](=[O:13])[CH2:11][C:5]1[C:4]2[C:8](=[CH:9][CH:10]=[C:2]([C:18]3[S:17][CH:21]=[CH:20][CH:19]=3)[CH:3]=2)[NH:7][CH:6]=1

参加物

6

反応物 4

HCID 10796Cesium carbonate2 回HCID 14798Sodium HydroxideHCID 27339602-Thiopheneboronic acidHCID 104464242-(5-bromo-1H-indol-3-yl)-N,N-dimethyl-acetamide

生成物 1

HCID 10356535N,N-Dimethyl-2-(5-thiophen-2-yl-1H-indol-3-yl)-acetamide収率 54%

試薬・触媒・溶媒 1

HCID 80711,2-Dimethoxyethane溶媒

実験手順

A solution of 2-(5-bromo-1H-indol-3-yl)-N,N-dimethyl-acetamide (Example 2) (227 mg, 0.81 mmol) in DME (5 mL) is degassed by sparging with argon for 10 minutes. Then thiophene-2-boronic acid (155 mg, 1.21 mmol), caesium carbonate (658 mg, 2.02 mmol), and π-allyl tri-isopropylphosphino palladium bromide (15.7 mg, 0.04 mmol) are added, and the mixture is heated under reflux. Two additional portions of caesium carbonate (103 mg, 0.81 mmol) are added after 20 hours and 24 hours to bring the reaction to completion. The black reaction mixture is poured into 2 N NaOH (10 mL), and extracted twice with ethyl acetate. After removal of the solvent, the residue is chromatographed on silica (CHCl3:MeOH 29:1 v:v) to give the title product (121 mg, 54%). 1H-NMR (CDCl3, 300 MHz) δ 2.96, 2.98 (2 s, 3H each, 2 CH3); 3.77 (s, 2H, CH2); 6.84 (d, 3J=2.2 Hz, H-2); 7.06 (dd, 3J=5.0 Hz, 3J=3.6 Hz, thiophene H-4); 7.21 (d, thiophene H-5); 7.21 (d, 3J=8.4 Hz, H-7); 7.25 (d, thiophene H-3); 7.40 (dd, 4J=1.8 Hz, H-6); 7.70 (d, H-4); 9.16 (br s, NH). 13C-NMR (CDCl3, 75 MHz) δ 31.02 (CH2); 36.00, 38.00 (2 CH3); 109.05 (C-3); 112.17 (C-7); 116.22 (C-4); 121.08 (C-6); 122.25 (thiophene C-3); 123.70 (thiophene C-5); 124.31 (C-2); 126.29 (thiophene C-2); 127.83 (C-9); 128.15 (thiophene C-4); 136.27 (C-8); 146.56 (C-5); 172.16 (CO).

後処理

  1. customby sparging with argon for 10 minutes
  2. temperaturethe mixture is heated
  3. temperatureunder reflux
  4. customthe reaction to completion
  5. customThe black reaction mixture
  6. extractionextracted twice with ethyl acetate
  7. customAfter removal of the solvent
  8. customthe residue is chromatographed on silica (CHCl3:MeOH 29:1 v:v)

出典と根拠

ORDレコード
ord-2bb4fa81cfb54aca809a4b224b83ac90
出典データセット
uspto-grants-2011_06
特許番号
US07968730B2

反応ノート

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