Hydrochloric Acid → 1-((3aR,4S,6aS)-4-aminohexahydrocyclopenta[c]pyrrol-2(1H)-yl)-3-methyl-2-phenylbutan-1-one hydrochloric acid salt
반응식
[CH3:1][CH:2]([CH3:28])[CH:3]([C:22]1[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=1)[C:4]([N:6]1[CH2:10][C@@H:9]2[C@@H:11]([NH:14]C(=O)OC(C)(C)C)[CH2:12][CH2:13][C@@H:8]2[CH2:7]1)=[O:5].[ClH:29].O1CCOCC1>CCOCC>[ClH:29].[NH2:14][C@@H:11]1[C@@H:9]2[C@@H:8]([CH2:7][N:6]([C:4](=[O:5])[CH:3]([C:22]3[CH:23]=[CH:24][CH:25]=[CH:26][CH:27]=3)[CH:2]([CH3:28])[CH3:1])[CH2:10]2)[CH2:13][CH2:12]1참가 물질
5
반응물 3
생성물 1
시약·촉매·용매 1
실험 절차
tert-Butyl(3aR,4S,6aS)-2-(3-methyl-2-phenylbutanoyl)octahydrocyclopenta[c]pyrrol-4-ylcarbamate (39 mg, 0.101 mmol) from Step C was combined with 4 M HCl in dioxane (5 mL, 20.00 mmol) in ether (5 mL). After about 2 hours, the solvent was removed in vacuo to give 1-((3aR,4S,6aS)-4-aminohexahydrocyclopenta[c]pyrrol-2(1H)-yl)-3-methyl-2-phenylbutan-1-one hydrochloric acid salt which was used in the next step without additional purification: MS (ESI+) m/z 287 (M+H)+.
후처리
- customthe solvent was removed in vacuo
출처 및 근거
- ORD 기록
- ord-02b034d125554e5dafa70dc355a9a590
- 출처 데이터셋
- uspto-grants-2014_04
- 특허 번호
- US08691865B2
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