Hydrochloric Acid → 5-{4-Oxospiro[chroman-2,4'-piperidin]-6-yl}nicotinic acid di-hydrochloride
반응식
C([O:5][C:6](=[O:36])[C:7]1[CH:12]=[C:11]([C:13]2[CH:14]=[C:15]3[C:32](=[CH:33][CH:34]=2)[O:31][C:18]2([CH2:23][CH2:22][N:21](C(OC(C)(C)C)=O)[CH2:20][CH2:19]2)[CH2:17][C:16]3=[O:35])[CH:10]=[N:9][CH:8]=1)(C)(C)C.[ClH:37]>C(Cl)(Cl)Cl.O1CCOCC1>[ClH:37].[ClH:37].[O:35]=[C:16]1[C:15]2[C:32](=[CH:33][CH:34]=[C:13]([C:11]3[CH:10]=[N:9][CH:8]=[C:7]([CH:12]=3)[C:6]([OH:36])=[O:5])[CH:14]=2)[O:31][C:18]2([CH2:23][CH2:22][NH:21][CH2:20][CH2:19]2)[CH2:17]1참가 물질
5
실험 절차
5-{1′-tert-butoxycarbonyl-4-oxospiro[chroman-2,4′-piperidin]-6-yl}nicotinic acid tert-butyl ester (14.0 g, 28.3 mmol) was dissolved in CHCl3 (70 mL) and 4N HCl in dioxane (210 mL) was added thereto, and stirred at room temperature for 20 h. The resulted precipitate was filtered and washed with CHCl3 and Et2O to afford 5-{4-oxospiro[chroman-2,4′-piperidin]-6-yl}nicotinic acid di-hydrochloride as a colorless solid.
후처리
- filtrationThe resulted precipitate was filtered
- washwashed with CHCl3 and Et2O
출처 및 근거
- ORD 기록
- ord-fcb54009207142dab0aafcf7c67ce897
- 출처 데이터셋
- uspto-grants-2012_03
- 특허 번호
- US08138197B2
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