반응식
[C:1]([NH:8][C@H:9]([C:11]([NH:13][C@H:14]([C:16]([OH:18])=O)[CH3:15])=[O:12])[CH3:10])([O:3][C:4]([CH3:7])([CH3:6])[CH3:5])=[O:2].CN1CCOCC1.[NH2:26][CH2:27][CH2:28][CH2:29][OH:30]>C1COCC1>[NH:8]([C:1]([O:3][C:4]([CH3:5])([CH3:6])[CH3:7])=[O:2])[C@H:9]([C:11]([NH:13][C@H:14]([C:16]([NH:26][CH2:27][CH2:28][CH2:29][OH:30])=[O:18])[CH3:15])=[O:12])[CH3:10]참가 물질
실험 절차
To a vigorously stirring solution of Boc-(Ala)2-OH (1.55 gm, 5.96 mmol) and NMM (0.98 mL, 8.9 mmol) in THF (15 mL) cooled to −15° C. was added under an atmosphere of N2 ethyl chloroformate (ECF) (587 μL, 6.14 mmol). After stirring for 2 min, a solution of H2N(CH2)3OH (546 uL, 7.2 mmol) in THF (5 mL) was added to the mixture followed by NMM (1.64 mL, 14.9 mmol) and the mixture was warmed to r.t. and stirred until silica gel TLC indicated complete consumption of the starting acid (eluting solvent-MeOH:DCM—1:10, Rf—0.5) (˜8 h). The solvent was evaporated, and the residue was diluted with EtOAc and washed with brine, water, saturated solutions of citric acid and NaHCO3, and the organic layer was dried using NaHSO4, and the solvent was removed under vacuum to yield a residue which was purified using silica gel flash column chromatography—Hexanes:EtOAc—1:4; to give the desired product in 84% yield (1.59 g) as a solid, m.p.—142° C.
후처리
- additionwas added under an atmosphere of N2 ethyl chloroformate (ECF) (587 μL, 6.14 mmol)
- stirringstirred until silica gel
- customconsumption of the starting acid (eluting solvent-MeOH:DCM—1:10, Rf—0.5) (˜8 h)
- customThe solvent was evaporated
- additionthe residue was diluted with EtOAc
- washwashed with brine, water, saturated solutions of citric acid and NaHCO3
- customthe organic layer was dried
- customthe solvent was removed under vacuum
- customto yield a residue which
- customwas purified
출처 및 근거
- ORD 기록
- ord-b033a9c4a8184099ba6d29d17aaf0d1a
- 출처 데이터셋
- uspto-grants-2014_09
- 특허 번호
- US08835602B2
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