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

HRID 1246437
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HRID 1246437 반응식
[Br:1][CH2:2][C:3](=O)[C:4]([O:6][CH2:7][CH3:8])=[O:5].[NH2:10][C:11]([NH2:13])=[S:12]>C(O)C>[BrH:1].[NH2:13][C:11]1[S:12][CH:2]=[C:3]([C:4]([O:6][CH2:7][CH3:8])=[O:5])[N:10]=1
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참가 물질

4

반응물 2

HCID 66144Ethyl bromopyruvateHCID 2723790Thiourea

생성물 1

HCID 16495520Ethyl 2-aminothiazole-4-carboxylate hydrobromide수율 89.4%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

A mixture of ethyl 3-bromo-2-oxopropanoate (100 g), thiourea (39 g) and ethanol (500 ml) was refluxed for 2 hours. The reaction mixture was concentrated in vacuo. The crystalline residue was collected and washed with ethyl acetate to give ethyl 2-amino-1,3-thiazole-4-carboxylate hydrobromide (116 g).

후처리

  1. temperaturewas refluxed for 2 hours
  2. concentrationThe reaction mixture was concentrated in vacuo
  3. customThe crystalline residue was collected
  4. washwashed with ethyl acetate

출처 및 근거

ORD 기록
ord-5e55cb4cb8894543824c526db6b5de81
출처 데이터셋
uspto-grants-2006_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07125901B2

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