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

HRID 460188
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HRID 460188 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]>CCO>[BrH:5].[CH2:11]([O:10][C:8]([C:7]1[N:1]=[C:2]([NH2:4])[S:3][CH:6]=1)=[O:9])[CH3:12]
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참가 물질

4

반응물 2

HCID 66144Ethyl bromopyruvateHCID 2723790Thiourea

생성물 1

HCID 16495520Ethyl 2-aminothiazole-4-carboxylate hydrobromide

시약·촉매·용매 1

HCID 702Ethanol용매

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온도
45 °C

실험 절차

To a stirred suspension of thiourea (24.26 g, 0.319 mol) in 200 proof EtOH (350 mL) at RT, under N2, ethyl bromopyruvate (62.16 g, 0.319 mol) was added dropwise. Upon completion the yellow solution was heated to 45° C. for 15 h, then placed in a fridge overnight. The precipitate was filtered off and washed with cold EtOH (3×100 mL) to yield the title compound as a pale yellow amorphous solid. MS m/z: 173.1 (M+H), 195.1 (M+Na). Calc'd. for C6H9BrN2O2S-253.12.

후처리

  1. filtrationThe precipitate was filtered off
  2. washwashed with cold EtOH (3×100 mL)

출처 및 근거

ORD 기록
ord-f5975fd286cc49ff8034f028dfb50512
출처 데이터셋
uspto-grants-2007_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07196104B2

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