Ammonium Chloride → tert-butyl (6R,7R)-7-(3,4-dichlorophenyl)-6-[(methylsulfonyl)carbamoyl]-1,4-oxazepane-4-carboxylate
반응식
[C:1]([O:5][C:6]([N:8]1[CH2:14][C@@H:13]([C:15](O)=[O:16])[C@H:12]([C:18]2[CH:23]=[CH:22][C:21]([Cl:24])=[C:20]([Cl:25])[CH:19]=2)[O:11][CH2:10][CH2:9]1)=[O:7])([CH3:4])([CH3:3])[CH3:2].[CH3:26][S:27]([NH2:30])(=[O:29])=[O:28].CC1C=CC=C([N+]([O-])=O)C=1C(OC(=O)C1C([N+]([O-])=O)=CC=CC=1C)=O.[Cl-].[NH4+]>C(#N)C.CN(C1C=CN=CC=1)C>[Cl:25][C:20]1[CH:19]=[C:18]([C@@H:12]2[O:11][CH2:10][CH2:9][N:8]([C:6]([O:5][C:1]([CH3:4])([CH3:3])[CH3:2])=[O:7])[CH2:14][C@H:13]2[C:15](=[O:16])[NH:30][S:27]([CH3:26])(=[O:29])=[O:28])[CH:23]=[CH:22][C:21]=1[Cl:24]참가 물질
7
반응물 4
생성물 1
시약·촉매·용매 2
실험 절차
To a solution of (6R,7R)-4-(tert-butoxycarbonyl)-7-(3,4-dichlorophenyl)-1,4-oxazepane-6-carboxylic acid (590 mg) in acetonitrile (15.1 mL) were added N,N-dimethyl-4-aminopyridine (203 mg), methanesulfonamide (158 mg) and 2-methyl-6-nitrobenzoic anhydride (625 mg) at room temperature, and the mixture was stirred at room temperature for 2 hr. To the reaction mixture was added aqueous ammonium chloride solution, and the mixture was extracted with ethyl acetate. The extract was washed with distilled water and brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel chromatography (hexane/ethyl acetate) to give the title compound (323 mg).
후처리
- extractionthe mixture was extracted with ethyl acetate
- washThe extract was washed with distilled water and brine
- dry with materialdried over anhydrous magnesium sulfate
- customThe solvent was evaporated under reduced pressure
- customthe residue was purified by silica gel chromatography (hexane/ethyl acetate)
출처 및 근거
- ORD 기록
- ord-d535f10a6c344f2aa24ff8c90fbeb8c8
- 출처 데이터셋
- uspto-grants-2014_05
- 특허 번호
- US08722662B2
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