(2S,4R)-2-((1S 2R)1-Ethoxycarbonyl-2-vinyl-cyclopropylcarbamoyl)-4-hydroxy-pyrrolidine-1-carboxylic acid tert.butyl ester → (1S,2R)-1-[(2S,4R)-(4-Hydroxy-pyrrolidine-2-carbonyl)-amino]-2-vinyl-cyclopropanecarboxylic acid ethyl ester
반응식
C(OC([N:8]1[CH2:12][C@H:11]([OH:13])[CH2:10][C@H:9]1[C:14](=[O:26])[NH:15][C@@:16]1([C:21]([O:23][CH2:24][CH3:25])=[O:22])[CH2:18][C@@H:17]1[CH:19]=[CH2:20])=O)(C)(C)C>FC(F)(F)C(O)=O.ClCCl>[CH2:24]([O:23][C:21]([C@:16]1([NH:15][C:14]([C@@H:9]2[CH2:10][C@@H:11]([OH:13])[CH2:12][NH:8]2)=[O:26])[CH2:18][C@@H:17]1[CH:19]=[CH2:20])=[O:22])[CH3:25]참가 물질
4
반응물 1
생성물 1
시약·촉매·용매 2
실험 절차
Compound 90 was kept in 30% trifluoroacetic acid in dichloromethane and 1% MeOH for 2 hrs before it was concentrated to dryness. The residue was re-dissolved In dichloromethane and during stirring 1N NaOH was added to pH 10-11. The organic layer was separated and concentrated which gave 1.6 g of the title product. HPLC purity ca. 90% M+H+269.1.
후처리
- concentration1% MeOH for 2 hrs before it was concentrated to dryness
- dissolutionThe residue was re-dissolved In dichloromethane
- additionwas added to pH 10-11
- customThe organic layer was separated
- concentrationconcentrated which
출처 및 근거
- ORD 기록
- ord-36bb4b666b954c26a78d5676a580b0ad
- 출처 데이터셋
- uspto-grants-2009_10
- 특허 번호
- US07608590B2
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