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Thiourea → Ethyl 2-amino-4-(propan-2-yl)-1,3-thiazole-5-carboxylate

HRID 1422398
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HRID 1422398 반응식
[NH2:1][C:2]([NH2:4])=[S:3].Br[CH:6]([C:12](=O)[CH:13]([CH3:15])[CH3:14])[C:7]([O:9][CH2:10][CH3:11])=[O:8]>C(O)C>[NH2:1][C:2]1[S:3][C:6]([C:7]([O:9][CH2:10][CH3:11])=[O:8])=[C:12]([CH:13]([CH3:15])[CH3:14])[N:4]=1
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참가 물질

4

반응물 2

HCID 2723790ThioureaHCID 13015595Ethyl 2-bromo-4-methyl-3-oxopentanoate

생성물 1

HCID 824436Ethyl 2-amino-4-(propan-2-yl)-1,3-thiazole-5-carboxylate수율 40.6%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

A solution of thiourea (1.1 g) in ethanol (10 mL) was brought to reflux. Ethyl 2-bromo-4-methyl-3-oxopentanoate (3.0 g) was then added and the reaction mixture refluxed further for 1 h. The reaction was complete (by TLC) and was concentrated in vacuum. Flash chromatography (100% DCM→90:10 DCM:MeOH) afforded the product (1.1 g).

후처리

  1. temperatureto reflux
  2. temperaturethe reaction mixture refluxed further for 1 h
  3. concentrationwas concentrated in vacuum

출처 및 근거

ORD 기록
ord-757bce8d5c33420980255c8d8a6e7596
출처 데이터셋
uspto-grants-2015_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
USRE045323E1

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