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Ethyl bromopyruvate → Ethyl 2-aminothiazole-4-carboxylate hydrobromide

HRID 1107080
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HRID 1107080 반응식
[NH2:1][C:2]([NH2:4])=[S:3].[Br:5][CH2:6][C:7](=O)[C:8]([O:10][CH2:11][CH3:12])=[O:9]>C(O)C>[BrH:5].[NH2:1][C:2]1[S:3][CH:6]=[C:7]([C:8]([O:10][CH2:11][CH3:12])=[O:9])[N:4]=1
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참가 물질

4

반응물 2

HCID 66144Ethyl bromopyruvateHCID 2723790Thiourea

생성물 1

HCID 16495520Ethyl 2-aminothiazole-4-carboxylate hydrobromide수율 79.2%

시약·촉매·용매 1

HCID 702Ethanol용매

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온도
45 °C

실험 절차

To a stirring suspension of thiourea (6.0 g, 78.8 mmol) in ethanol (80 mL) was added ethyl bromopyruvate (15.4 g, 78.8 mmol). The resulting solution was heated at 45° C. for 23 h. The solution was cooled at 0° C. for 24 h, and the crystals were collected by filtration and washed with cold ethanol to provide the title compound (15.8 g, 79%). 1H NMR (400 MHz, CD3OD) δ7.70 (s, 1H), 4.41 (q, 2H), 1.38 (t, 3H).

후처리

  1. temperatureThe solution was cooled at 0° C. for 24 h
  2. filtrationthe crystals were collected by filtration
  3. washwashed with cold ethanol

출처 및 근거

ORD 기록
ord-2b4ed290fab44c49bed704f73787ce9b
출처 데이터셋
uspto-grants-2000_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06057362

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