Triethylamine → 2-[(4'-Methoxy[1,1'-biphenyl]-4-yl)sulfonyl]amino-4-hydroxy-5-[(2-thiazolyl)thio]-pentanoic Acid

HRID 413358노트

반응식

HRID 413358 반응식
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([C:9]2[CH:14]=[CH:13][C:12]([S:15]([NH:18][CH:19]([CH2:24][CH:25]3[O:27][CH2:26]3)[C:20]([O:22]C)=[O:21])(=[O:17])=[O:16])=[CH:11][CH:10]=2)=[CH:5][CH:4]=1.CCN(CC)CC.[SH:35][C:36]1[S:37][CH:38]=[CH:39][N:40]=1>C1C=CC=CC=1.O>[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([C:9]2[CH:10]=[CH:11][C:12]([S:15]([NH:18][CH:19]([CH2:24][CH:25]([OH:27])[CH2:26][S:35][C:36]3[S:37][CH:38]=[CH:39][N:40]=3)[C:20]([OH:22])=[O:21])(=[O:17])=[O:16])=[CH:13][CH:14]=2)=[CH:5][CH:4]=1

참가 물질

6

실험 절차

To a solution of methyl 2-[(4′-methoxy[1,1′-biphenyl]-4-yl)sulfonyl]amino-4,5-epoxypentanoate 1d (0.7 g, 1.79 mmol) in benzene (5 mL) and Et3N (0.33 mL, 2.3 mmol) at room temperature is added slowly 2-mercaptothiazole (0.52 g, 4.48 mmol). The reaction mixture is stirred for 4 h at room temperature. The resulting mixture is diluted with water, and the mixture is then extracted three times with EtOAc. The combined EtOAc layer is consecutively washed with water, and brine, dried over MgSO4 and concentrated to an oil under reduced pressure. Purification is accomplished by column chromatography with hexane/EtOAc (4:1 to 7:3 to 6:4) eluent to give the desired product.

후처리

  1. extractionthe mixture is then extracted three times with EtOAc
  2. washThe combined EtOAc layer is consecutively washed with water, and brine
  3. dry with materialdried over MgSO4
  4. concentrationconcentrated to an oil under reduced pressure
  5. customPurification

출처 및 근거

ORD 기록
ord-ab1c37af08ed4c42af1536ea8a727798
출처 데이터셋
uspto-grants-2003_05
특허 번호
US06566381B1

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