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Ethyl thiooxamate → Ethyl 4-[3-(trifluoromethyl)phenyl]-1,3-thiazole-2-carboxylate

HRID 1257462
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인쇄 미리보기

반응식

HRID 1257462 반응식
Br[CH2:2][C:3]([C:5]1[CH:10]=[CH:9][CH:8]=[C:7]([C:11]([F:14])([F:13])[F:12])[CH:6]=1)=O.[NH2:15][C:16](=[S:22])[C:17]([O:19][CH2:20][CH3:21])=[O:18]>>[F:12][C:11]([F:14])([F:13])[C:7]1[CH:6]=[C:5]([C:3]2[N:15]=[C:16]([C:17]([O:19][CH2:20][CH3:21])=[O:18])[S:22][CH:2]=2)[CH:10]=[CH:9][CH:8]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 2733398Ethyl thiooxamateHCID 27783862-Bromo-1-[3-(trifluoromethyl)phenyl]ethan-1-one

생성물 1

HCID 10424923Ethyl 4-[3-(trifluoromethyl)phenyl]-1,3-thiazole-2-carboxylate수율 49%

반응 조건

온도
80 °C

실험 절차

To 2-bromo-1-[3-(trifluoromethyl)phenyl]ethanone (14 g, 41 mmol) was added ethyl amino(thioxo)acetate (5.0 g, 38 mmol), and the mixture was stirred at 80° C. for 3 hr. The solvent was evaporated under reduced pressure, and the obtained crude product was purified by recrystallization (ethyl acetate) to give the title compound (5.6 g, 49%) as colorless crystals.

후처리

  1. customThe solvent was evaporated under reduced pressure
이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트
  • customthe obtained crude product
  • customwas purified by recrystallization (ethyl acetate)
  • 출처 및 근거

    ORD 기록
    ord-24e1736126a041aea6279d4158432356
    출처 데이터셋
    uspto-grants-2013_06
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US08461348B2

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