반응식
[C:1]([NH:8][S:9]([C:12]1[CH:17]=[CH:16][C:15]([CH3:18])=[CH:14][CH:13]=1)(=[O:11])=[O:10])(OC(C)(C)C)=O.C1C=CC(P(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1.OC[CH:40]=[CH:41][C:42]1[CH:64]=[CH:63][C:45]([C:46]([NH:48][C:49]2[CH:54]=[CH:53][CH:52]=[CH:51][C:50]=2[NH:55][C:56](=[O:62])[O:57][C:58]([CH3:61])([CH3:60])[CH3:59])=[O:47])=[CH:44][CH:43]=1.N(C(OCC)=O)=NC(OCC)=O>C1COCC1>[C:15]1([CH3:18])[CH:14]=[CH:13][C:12]([S:9]([NH:8][CH2:1][CH:40]=[CH:41][C:42]2[CH:64]=[CH:63][C:45]([C:46]([NH:48][C:49]3[CH:54]=[CH:53][CH:52]=[CH:51][C:50]=3[NH:55][C:56](=[O:62])[O:57][C:58]([CH3:59])([CH3:60])[CH3:61])=[O:47])=[CH:44][CH:43]=2)(=[O:10])=[O:11])=[CH:17][CH:16]=1참가 물질
6
반응물 4
생성물 1
시약·촉매·용매 1
실험 절차
To a stirred solution of N-Boc-4-tolylsulfonamide (221 mg, 0.81 mmol) and PPh3 (427 mg, 1.63 mmol) in anhydrous THF (4 ml) under nitrogen was successively added a solution of compound XVIII (200 mg, 0.54 mmol) in anhydrous THF (1 ml) and diethyl azodicarboxylate (DEAD) (214 μl, 1.36 mmol). After 16 h, the reaction mixture was quenched with water and diluted with AcOEt. After separation the organic layer was successively washed with water and brine, dried over MgSO4, filtered, and concentrated. The crude residue was then purified by flash chromatography on silica gel (AcOEt/hexane:40/60) to afford the title compound XVIIg (337 mg).
후처리
- customthe reaction mixture was quenched with water
- additiondiluted with AcOEt
- customAfter separation the organic layer
- washwas successively washed with water and brine
- dry with materialdried over MgSO4
- filtrationfiltered
- concentrationconcentrated
- customThe crude residue was then purified by flash chromatography on silica gel (AcOEt/hexane:40/60)
출처 및 근거
- ORD 기록
- ord-57d4d008feba4e459f148af7837eafeb
- 출처 데이터셋
- uspto-grants-2007_10
- 특허 번호
- US07282608B2
연결된 노트
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