반응식
[F:1][C:2]1([F:18])[CH2:6][N:5](C(OC(C)(C)C)=O)[C@H:4]([C:14]([O:16][CH3:17])=[O:15])[CH2:3]1.FC(F)(F)C(O)=O>C(Cl)Cl>[F:18][C:2]1([F:1])[CH2:6][NH:5][C@H:4]([C:14]([O:16][CH3:17])=[O:15])[CH2:3]1참가 물질
4
실험 절차
(S)-1-tert-butyl 2-methyl 4,4-difluoropyrrolidine-1,2-dicarboxylate (0.472 g) in CH2Cl2 (1 mL) was treated with trifluoroacetic acid (1.4 mL), stirred at ambient temperature for 4 hours, and concentrated. The product was free-based using a MEGA BE-SCX column with 1:1 CH2Cl2/methanol as eluent for the trifluoroacetic acid. The product was released from the column with 5% (7 M ammonia in methanol) in CH2Cl2 as eluent.
후처리
- concentrationconcentrated
출처 및 근거
- ORD 기록
- ord-b635a8837e8847eca488274e5fbc6221
- 출처 데이터셋
- uspto-grants-2013_10
- 특허 번호
- US08546399B2
연결된 노트
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