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Isopropanol → Methyl 4-(2-aminothiazol-4-yl)benzoate

HRID 1889187
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반응식

HRID 1889187 반응식
[CH3:1][O:2][C:3](=[O:14])[C:4]1[CH:9]=[CH:8][C:7]([C:10](=O)[CH2:11]Br)=[CH:6][CH:5]=1.[NH2:15][C:16]([NH2:18])=[S:17].C(O)(C)C.C(=O)([O-])[O-].[Na+].[Na+]>O>[CH3:1][O:2][C:3](=[O:14])[C:4]1[CH:9]=[CH:8][C:7]([C:10]2[N:15]=[C:16]([NH2:18])[S:17][CH:11]=2)=[CH:6][CH:5]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 3776IsopropanolHCID 10340Sodium CarbonateHCID 2723790ThioureaHCID 13612771Methyl 4-(2-bromoacetyl)benzoate

생성물 1

HCID 2060012Methyl 4-(2-aminothiazol-4-yl)benzoate수율 55%

시약·촉매·용매 1

HCID 962Water용매

실험 절차

A mixture of 4-(2-bromo-acetyl)-benzoic acid methyl ester (1 g, 3.89 mmol) and thiourea (0.29 g, 3.89 mmol) were taken isopropyl alcohol (100 ml) and refluxed for 10 minutes followed by addition of sodium carbonate (0.206 g, 1.94 mmol) and stirred for 30 minutes. Reaction mixture was cooled to room temperature and poured in water. The precipitate obtained was filtered off, washed with water and diethyl ether and dried under vacuum to afford 4-(2-amino-thiazol-4-yl)-benzoic acid methyl ester (0.500 g, 55%).

후처리

  1. temperaturerefluxed for 10 minutes
  2. customReaction mixture
  3. customThe precipitate obtained
  4. filtrationwas filtered off
  5. washwashed with water and diethyl ether
  6. customdried under vacuum

출처 및 근거

ORD 기록
ord-edd68001d0254201baf403bffba13558
출처 데이터셋
uspto-grants-2013_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08501955B2

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