1-Hydroxybenzotriazole → Tert-butyl 4-({[2-(acetylamino)-1,3-thiazol-4-yl]carbonyl)amino}phenylcarbamate

HRID 2117850노트

반응식

HRID 2117850 반응식
[C:1]([NH:4][C:5]1[S:6][CH:7]=[C:8]([C:10]([OH:12])=O)[N:9]=1)(=[O:3])[CH3:2].[NH2:13][C:14]1[CH:19]=[CH:18][C:17]([NH:20][C:21](=[O:27])[O:22][C:23]([CH3:26])([CH3:25])[CH3:24])=[CH:16][CH:15]=1.Cl.C(N=C=NCCCN(C)C)C.ON1C2C=CC=CC=2N=N1>ClCCl>[C:1]([NH:4][C:5]1[S:6][CH:7]=[C:8]([C:10]([NH:13][C:14]2[CH:15]=[CH:16][C:17]([NH:20][C:21](=[O:27])[O:22][C:23]([CH3:25])([CH3:24])[CH3:26])=[CH:18][CH:19]=2)=[O:12])[N:9]=1)(=[O:3])[CH3:2]

참가 물질

6

실험 절차

A mixture of 2-(acetylamino)-1,3-thiazole-4-carboxylic acid (500 mg), tert-butyl 4-aminophenylcarbamate (615 mg), 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (566 mg), 1-hydroxybenzotriazole (399 mg) and dichloromethane (5 ml) was stirred at ambient temperature for 3 hours. The reaction mixture was washed with saturated aqueous sodium hydrogen bicarbonate, and the organic layer was concentrated in vacuo. The residue was purified by flash column chromatography on silica gel with 3% methanol/chloroform as an eluent. The crystalline residue was collected and washed with ethyl acetate to give tert-butyl 4-({[2-(acetylamino)-1,3-thiazol-4-yl]carbonyl}amino)phenylcarbamate (580 mg).

후처리

  1. washThe reaction mixture was washed with saturated aqueous sodium hydrogen bicarbonate
  2. concentrationthe organic layer was concentrated in vacuo
  3. customThe residue was purified by flash column chromatography on silica gel with 3% methanol/chloroform as an eluent
  4. customThe crystalline residue was collected
  5. washwashed with ethyl acetate

출처 및 근거

ORD 기록
ord-c6042cca903d4a898dec2b37e56d7388
출처 데이터셋
uspto-grants-2008_10
특허 번호
US07442715B2

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