Hydroxylamine → ((1S,4S)-5-Benzhydryl-2,5-diazabicyclo[2.2.1]heptan-2-yl)-N-hydroxypyrimidine-5-carboxamide
反応式
[CH:1]([N:14]1[CH2:19][C@@H:18]2[CH2:20][C@H:15]1[CH2:16][N:17]2[C:21]1[N:26]=[CH:25][C:24]([C:27](OCC)=[O:28])=[CH:23][N:22]=1)([C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[OH-:32].[K+].[NH2:34]O.CO>C1COCC1>[CH:1]([N:14]1[CH2:19][C@@H:18]2[CH2:20][C@H:15]1[CH2:16][N:17]2[C:21]1[N:26]=[CH:25][C:24]([C:27]([NH:34][OH:32])=[O:28])=[CH:23][N:22]=1)([C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1)[C:8]1[CH:9]=[CH:10][CH:11]=[CH:12][CH:13]=1参加物
6
反応物 4
生成物 1
試薬・触媒・溶媒 1
実験手順
Title compound 202 (0.140 g, 0.338 mmol), potassium hydroxide (4M, 0.34 mL), hydroxylamine (50% in water, 0.34 mL), MeOH (2 mL) and THF (2 mL) were combined and the reaction mixture was stirred for 1 hour. HCL 3N was added to adjust the pH to 8. After 15 minutes stirring, the solid was filtered and well dried to afford the title compound 203 (0.107 g, 79%) as a white powder. 1H NMR (DMSO-d6) δ (ppm): 7.80 (dd, J=8.0, 2.0 Hz, 1H), 7.61 (ddd, J=8.4, 6.8, 1.2 Hz, 1H), 7.46-7.41 (m, 3H), 7.38-7.30 (m, 3H), 3.62 (t, J=7.2 Hz, 2H), 2.06 (t, J=7.2 Hz, 2H), 1.61-1.51 (m, 4H), 1.44-1.28 (m, 4H). LRMS: (calc) 390.12. (found) 391.3 (MH)+.
後処理
- additionHCL 3N was added
- stirringAfter 15 minutes stirring
- filtrationthe solid was filtered
- customwell dried
出典と根拠
- ORDレコード
- ord-6dca1167f4b54489807d1bf73dbb5c9f
- 出典データセット
- uspto-grants-2015_11
- 特許番号
- US09193749B2
反応ノート
読み込み中…