Hydrochloric Acid → 4-Piperidyloxyamine dihydrochloride
反応式
C(OC([N:8]1[CH2:13][CH2:12][CH:11]([O:14][NH2:15])[CH2:10][CH2:9]1)=O)(C)(C)C.[ClH:16]>CCOC(C)=O>[ClH:16].[ClH:16].[NH:8]1[CH2:13][CH2:12][CH:11]([O:14][NH2:15])[CH2:10][CH2:9]1参加物
4
実験手順
1-tert-Butoxycarbonyl-4-piperidyloxyamine (120 mg) was dissolved in a 5M HCl solution in EtOAc (3 mL). After 1 h the solvent was removed under reduced pressure to give the title compound III-a (100 mg, 96%). 1H-NMR (300 MHz, DMSO-d6, ppm from TMS): δ 10.95 (3H, bb), 8.96 (2H, bb), 4.33 (1H, m), 3.13 (2H, m), 3.00 (2H, m), 2.09 (2H, m), 1.85 (2H, m).
後処理
- customAfter 1 h the solvent was removed under reduced pressure
出典と根拠
- ORDレコード
- ord-4f1d3b8d0921442ebe3202700f85034e
- 出典データセット
- uspto-grants-2013_09
- 特許番号
- US08536160B2
反応ノート
読み込み中…