Hydrochloric Acid → Ethyl trans-4-hydroxy-L-prolinate hydrochloride
반응식
[OH:1][C@H:2]1[CH2:6][NH:5][C@H:4]([C:7]([OH:9])=[O:8])[CH2:3]1.[ClH:10].[CH3:11][CH2:12]O>>[ClH:10].[CH2:11]([O:8][C:7](=[O:9])[C@@H:4]1[CH2:3][C@@H:2]([OH:1])[CH2:6][NH:5]1)[CH3:12]참가 물질
실험 절차
Trans-4-hydroxy-L-proline was treated with EtOH and HCl gas, and the mixture was evaporated to give trans-4-hydroxy-L-proline ethyl ester hydrochloride. This product was treated with TsCI and Et3N in CH2Cl2, to give after aqueous workup N-(toluene-4-sulfonyl)-trans-4-hydroxy-L-proline ethyl ester. This product was treated with morpholinosulfur trifluoride in CH2Cl2, to give after aqueous workup N-(toluene-4-sulfonyl)-cis-4-fluoro-L-proline ethyl ester. This product was treated with NaOH in CH3OH and H2O to give, after acidification, extraction, drying with MgSO4, filtration and evaporation, N-(toluene-4-sulfonyl)-cis-4-fluoro-L-proline. This product was treated with HCl.Phe-OBn, BOP, and NMM in DMF, to give after aqueous workup and flash chromatography the title compound as a clear oil.
후처리
- customthe mixture was evaporated
출처 및 근거
- ORD 기록
- ord-e639e42390f540678b5306d7b84e59aa
- 출처 데이터셋
- uspto-grants-2002_03
- 특허 번호
- US06362341B1
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