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Ethanol → N-{1,1-Dimethyl-2-[4-(2-methyl-thiazol-4-yl)phenyl]-ethyl}-2,2,2-trifluoroacetamide

HRID 49386
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인쇄 미리보기

반응식

HRID 49386 반응식
BrCC([C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][C:6]=1[CH2:11][C:12]([NH:15][C:16](=[O:21])[C:17]([F:20])([F:19])[F:18])([CH3:14])[CH3:13])=O.[C:22]([NH2:25])(=[S:24])[CH3:23].[CH2:26](O)[CH3:27]>>[CH3:14][C:12]([NH:15][C:16](=[O:21])[C:17]([F:18])([F:19])[F:20])([CH3:13])[CH2:11][C:6]1[CH:5]=[CH:10][C:9]([C:26]2[N:25]=[C:22]([CH3:23])[S:24][CH:27]=2)=[CH:8][CH:7]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 702EthanolHCID 2723949ThioacetamideHCID 18523616N[2-(Bromoacetyl-phenyl)-1,1-dimethyl-ethyl]-2,2,2-trifluoroacetamide

생성물 1

HCID 18523660N-{1,1-Dimethyl-2-[4-(2-methyl-thiazol-4-yl)phenyl]-ethyl}-2,2,2-trifluoroacetamide

반응 조건

온도
80 °C

실험 절차

In a round-bottomed flask, N-[2-(bromoacetyl-phenyl)-1,1-dimethyl-ethyl]-2,2,2-trifluoroacetamide (388 mg, 1.06 mmol) and thioacetamide (80 mg, 1.06 mmol) were dissolved in ethanol (10 ml), and the mixture was heated to about 80° C. for about two and one-half hours. The reaction mixture was then concentrated in vacuo to an oil which was carried into the next reaction without further purification. LRMS ([M+1]+)=343.2.

후처리

  1. concentrationThe reaction mixture was then concentrated in vacuo to an oil which
  2. customwas carried into the next reaction without further purification

출처 및 근거

ORD 기록
ord-cec7ed45586644598f68d5c4d523dc3a
출처 데이터셋
uspto-grants-2004_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06706743B2

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