Hydroxyamine hydrochloride → HCID 178483044, 화합물
반응식
[ClH:1].[NH2:2][OH:3].C(=O)(O)[O-].[Na+].Cl[C:10]1[CH:11]=[C:12]([C:19]2[C:24]3[N:25]([CH2:37][C@H:38]4[CH2:43][CH2:42][C@H:41]([CH3:44])[CH2:40][CH2:39]4)[C:26]([N:28]4[CH2:33][CH2:32][O:31][C@@H:30]5[CH2:34][CH2:35][CH2:36][C@@H:29]45)=[N:27][C:23]=3[CH:22]=[C:21]([C:45]#[N:46])[N:20]=2)[C:13]([N:16]([CH3:18])[CH3:17])=[N:14][CH:15]=1>O.C(O)C>[Cl:1][C:10]1[CH:11]=[C:12]([C:19]2[C:24]3[N:25]([CH2:37][C@H:38]4[CH2:39][CH2:40][C@H:41]([CH3:44])[CH2:42][CH2:43]4)[C:26]([N:28]4[CH2:33][CH2:32][O:31][C@@H:30]5[CH2:34][CH2:35][CH2:36][C@@H:29]45)=[N:27][C:23]=3[CH:22]=[C:21]([C:45](=[NH:46])[NH:2][OH:3])[N:20]=2)[C:13]([N:16]([CH3:17])[CH3:18])=[N:14][CH:15]=1참가 물질
실험 절차
Hydroxylamine hydrochloride (4.3 mg, 0.07 mmol) and sodium bicarbonate (7 mg, 0.08 mmol) were dissolved in water (0.4 mL) and stirred at room temperature for 10 minutes, allowing gas to evolve. This solution was then added to a solution of 4-[5-chloro-2-(dimethylamino)pyridin-3-yl]-2-[(trans)-hexahydrocyclopenta[b][1,4]oxazin-4(4aH)-yl]-3-[(trans-4-methylcyclohexyl)methyl]-3H-imidazo[4,5-c]pyridine-6-carbonitrile (racemic, 26 mg, 0.05 mmol) in ethanol (0.2 mL). This reaction mixture was stirred at 90° C. for 1 hour. The reaction mixture was concentrated and diluted with water (2 mL). The solid was filtered off to afford (crude) 4-[5-chloro-2-(dimethylamino)pyridin-3-yl]-2-[(trans)-hexahydrocyclopenta[b][1,4]oxazin-4(4aH)-yl]-N-hydroxy-3-[(trans-4-methylcyclohexyl)methyl]-3H-imidazo[4,5-c]pyridine-6-carboximidamide (racemic). MS ES calc'd. for C29H39ClN8O2 [M+H]+ 567. found 567.
후처리
- stirringThis reaction mixture was stirred at 90° C. for 1 hour
- concentrationThe reaction mixture was concentrated
- additiondiluted with water (2 mL)
- filtrationThe solid was filtered off
출처 및 근거
- ORD 기록
- ord-8fdf1541072343dba66d6612d011eff9
- 출처 데이터셋
- uspto-grants-2015_02
- 특허 번호
- US08962611B2
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