Cesium carbonate → 1,1-Dimethylethyl [5-cyano-2-cyclopropyl-4-(trifluoromethyl)-1H-indol-1-yl]acetate

HRID 913756노트

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HRID 913756 반응식
[CH:1]1([C:4]2[NH:5][C:6]3[C:11]([CH:12]=2)=[C:10]([C:13]([F:16])([F:15])[F:14])[C:9]([C:17]#[N:18])=[CH:8][CH:7]=3)[CH2:3][CH2:2]1.C(=O)([O-])[O-].[Cs+].[Cs+].Br[CH2:26][C:27]([O:29][C:30]([CH3:33])([CH3:32])[CH3:31])=[O:28]>C(#N)C>[C:17]([C:9]1[C:10]([C:13]([F:14])([F:15])[F:16])=[C:11]2[C:6](=[CH:7][CH:8]=1)[N:5]([CH2:26][C:27]([O:29][C:30]([CH3:33])([CH3:32])[CH3:31])=[O:28])[C:4]([CH:1]1[CH2:2][CH2:3]1)=[CH:12]2)#[N:18]

참가 물질

5

반응물 3

HCID 10796Cesium carbonateHCID 79177tert-Butyl bromoacetateHCID 674044722-cyclopropyl-4-(trifluoromethyl)-1H-indole-5-carbonitrile

생성물 1

HCID 711086661,1-Dimethylethyl [5-cyano-2-cyclopropyl-4-(trifluoromethyl)-1H-indol-1-yl]acetate수율 84.4%

시약·촉매·용매 1

HCID 6342Acetonitrile용매

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온도
85 °C

실험 절차

To a solution of 2-cyclopropyl-4-(trifluoromethyl)-1H-indole-5-carbonitrile (Example 165A) (1.0 g, 4.0 mmol) in dry acetonitrile (25 mL) was added cesium carbonate (2.6 g, 8.0 mmol) and t-butyl bromoacetate (768 uL, 5.2 mmol) at rt. The mixture was stirred at 85° C. overnight. The solid was filtered and the filtrate was then concentrated in vacuo. The residue was triturated with EtOAc-hexane to afford the title compound (1.23 g) in quantitative yield: MS (ES) m/z 365 (M+1).

후처리

  1. filtrationThe solid was filtered
  2. concentrationthe filtrate was then concentrated in vacuo
  3. customThe residue was triturated with EtOAc-hexane

출처 및 근거

ORD 기록
ord-61654100b13d403b8a50993ad388304d
출처 데이터셋
uspto-grants-2011_09
특허 번호
US08026262B2

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