반응식
[CH3:1][C:2]1[O:6][C:5]([C:7]2[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=2)=[N:4][C:3]=1[CH2:13][CH2:14]Br.[SH:16][C:17]1[CH:18]=[C:19]([CH2:23][C:24]([OH:26])=[O:25])[CH:20]=[CH:21][CH:22]=1.C(=O)([O-])[O-].[K+].[K+]>C(#N)C>[CH3:1][C:2]1[O:6][C:5]([C:7]2[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=2)=[N:4][C:3]=1[CH2:13][CH2:14][S:16][C:17]1[CH:18]=[C:19]([CH2:23][C:24]([OH:26])=[O:25])[CH:20]=[CH:21][CH:22]=1참가 물질
5
실험 절차
2-(5-methyl-2-phenyloxazol-4-yl)ethylbromide (136 mg) and 3-mercaptophenylacetic acid.methyl ester (78 mg) were dissolved in acetonitrile (5 ml) and thereto was added potassium carbonate and the mixture was stirred at room temperature for 1 hour. The reaction mixture was poured into ice water and the mixture was extracted with ether. The extract was washed with an aqueous solution of sodium hydroxide, water and a saturated aqueous solution of sodium chloride, successively, dried over anhydrous magnesium sulfate and concentrated. The residue was purified by column chromatography on silica gel (chloroform:ethyl acetate=200:1→50:1) to give the compound of the present invention (92 mg) having the following physical data.
후처리
- extractionthe mixture was extracted with ether
- washThe extract was washed with an aqueous solution of sodium hydroxide, water
- dry with materiala saturated aqueous solution of sodium chloride, successively, dried over anhydrous magnesium sulfate
- concentrationconcentrated
- customThe residue was purified by column chromatography on silica gel (chloroform:ethyl acetate=200:1→50:1)
- customto give the compound of the present invention (92 mg)
출처 및 근거
- ORD 기록
- ord-e64951fedac248b5a1c2df2c983bd553
- 출처 데이터셋
- uspto-grants-2006_05
- 특허 번호
- US07037914B2
연결된 노트
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