Hydrochloric Acid → 5-aminomethyl-6-((S)-2-imidazol-1-yl-1-phenyl-ethoxy)-3,4-dihydro-2H-naphthalen-1-one bis-hydrochloride
반응식
C(OC(=O)[NH:7][CH2:8][C:9]1[C:18]2[CH2:17][CH2:16][CH2:15][C:14](=[O:19])[C:13]=2[CH:12]=[CH:11][C:10]=1[O:20][C@@H:21]([C:28]1[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=1)[CH2:22][N:23]1[CH:27]=[CH:26][N:25]=[CH:24]1)(C)(C)C.[ClH:35]>O1CCOCC1>[ClH:35].[ClH:35].[NH2:7][CH2:8][C:9]1[C:10]([O:20][C@@H:21]([C:28]2[CH:29]=[CH:30][CH:31]=[CH:32][CH:33]=2)[CH2:22][N:23]2[CH:27]=[CH:26][N:25]=[CH:24]2)=[CH:11][CH:12]=[C:13]2[C:18]=1[CH2:17][CH2:16][CH2:15][C:14]2=[O:19]참가 물질
4
반응물 2
생성물 1
시약·촉매·용매 1
실험 절차
[2-((S)-2-Imidazol-1-yl-1-phenyl-ethoxy)-5-oxo-5,6,7,8-tetrahydro-naphthalen-1-ylmethyl]-carbamic acid tert-butyl ester (0.830 g, 1.80 mmol) was dissolved in dioxane (10 mL) and 4M HCl in dioxane (4 mL) was added. After 15 minutes, a white precipitate formed. The precipitate was collected by filtration, washed with Et2O and dried in a vacuum oven to give the title compound as a white fluffy solid (0.761 g, 1.75 mmol, 97%). The structure was confirmed by NMR, mass spectrometry and elemental analysis. MS m/z 362 (M++H).
후처리
- customa white precipitate formed
- filtrationThe precipitate was collected by filtration
- washwashed with Et2O
- customdried in a vacuum oven
출처 및 근거
- ORD 기록
- ord-ccca1b05e02b4f12adf6cf3b0d90045e
- 출처 데이터셋
- uspto-grants-2005_09
- 특허 번호
- US06943183B2
반응 노트
불러오는 중…