반응식
C(OC([NH:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][NH:14][C:15]1[CH:24]=[CH:23][CH:22]=[C:21]2[C:16]=1[CH:17]=[CH:18][N:19]=[CH:20]2)=O)(C)(C)C.[ClH:25].CO>>[ClH:25].[CH:20]1[C:21]2[C:16](=[C:15]([NH:14][CH2:13][CH2:12][CH2:11][CH2:10][CH2:9][NH2:8])[CH:24]=[CH:23][CH:22]=2)[CH:17]=[CH:18][N:19]=1참가 물질
3
실험 절차
According to the method of the above Example, deprotection was performed (room temperature, 31 hours) by using Intermediate 31 (327 mg) and 10% hydrogen chloride/methanol solution (5 ml). The solvent was evaporated under reduced pressure, and the residue was added with methanol (1 ml) and diethyl ether (3 ml). The deposited precipitates were collected by filtration and washed with diethyl ether to obtain the title compound (262 mg) as light yellow powdery solid.
후처리
- custom(room temperature, 31 hours)
- customThe solvent was evaporated under reduced pressure
- additionthe residue was added with methanol (1 ml) and diethyl ether (3 ml)
- customThe deposited precipitates
- filtrationwere collected by filtration
- washwashed with diethyl ether
출처 및 근거
- ORD 기록
- ord-95aa8b8184824c4f92502d147d13a2fb
- 출처 데이터셋
- uspto-grants-2006_08
- 특허 번호
- US07094789B2
연결된 노트
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