Hydrogen chloride-ethyl acetate → Carbostyrilhydrochloride
反応式
O1C2C=CC(CN(C3CCN(CC[N:28]4[C:37]5[C:32](=[CH:33][CH:34]=[CH:35][CH:36]=5)[CH:31]=[CH:30][C:29]4=[O:38])CC3)C(=O)OC(C)(C)C)=CC=2OCC1.[ClH:39].C(OCC)(=O)C>>[ClH:39].[NH:28]1[C:37]2[C:32](=[CH:33][CH:34]=[CH:35][CH:36]=2)[CH:31]=[CH:30][C:29]1=[O:38]参加物
3
実験手順
To 0.13 g of tert-butyl (2,3-dihydro-1,4-benzodioxin-6-ylmethyl)(1-(2-(2-oxoquinolin-1(2H)-yl)ethyl)piperidin-4-yl)carbamate, 10 mL of 4 mol/L hydrogen chloride/ethyl acetate solution was added, and left to stand at room temperature for 3 days. The solvent was removed under reduced pressure, 2-propanol was added to the residue obtained and the solvent was removed under reduced pressure. Ethyl acetate was added to the residue thus obtained and the resulting solid was filtered to afford 0.10 g of 1-(2-(4-(2,3-dihydro-1,4-benzodioxin-6-ylmethyl)amino)piperidin-1-yl)ethyl)-quinolin-2(1H)one hydrochloride as a yellow solid.
後処理
- waitleft
- customThe solvent was removed under reduced pressure, 2-propanol
- additionwas added to the residue