반응식
C(OC(=O)[NH:7][CH2:8][CH2:9][CH2:10][CH2:11][N:12]1[CH2:22][CH2:21][C:20]2[C:23]3[CH:13]1[CH2:14][C:15](=[O:28])[C:16]=3[C:17]([O:26][CH3:27])=[C:18]([O:24][CH3:25])[CH:19]=2)(C)(C)C.[ClH:30]>C(Cl)Cl.C(O)C.CCOCC>[ClH:30].[ClH:30].[NH2:7][CH2:8][CH2:9][CH2:10][CH2:11][N:12]1[CH2:22][CH2:21][C:20]2[C:23]3[CH:13]1[CH2:14][C:15](=[O:28])[C:16]=3[C:17]([O:26][CH3:27])=[C:18]([O:24][CH3:25])[CH:19]=2참가 물질
6
반응물 2
생성물 1
시약·촉매·용매 3
실험 절차
[4-(7,8-Dimethoxy-1-oxo-2,2a,4,5-tetrahydro-1H-3-aza-acenaphthylen-3-yl)-butyl]-carbamic acid tert-butyl ester (498 mg, 1.22 mmol) is dissolved in a mixture of CH2Cl2 (10 ml) and ethanol (2 ml) and a solution of 2 N HCl in Et2O is added (6 ml, 12 mmol). A brown precipitate appears, which is collected by filtration (367 mg, 80% yield).
후처리
- filtrationwhich is collected by filtration (367 mg, 80% yield)
출처 및 근거
- ORD 기록
- ord-b6577182b20c48d481f6d107a2db4c2e
- 출처 데이터셋
- uspto-grants-2009_06
- 특허 번호
- US07553965B2
연결된 노트
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