Water → HCID 13533227、化合物
反応式
[CH3:1][N:2]1[C:12]2[C:7](=[C:8]([C:15](=[O:21])[CH2:16][NH:17][CH:18]([CH3:20])[CH3:19])[CH:9]=[CH:10][C:11]=2[O:13]C)[CH:6]=[CH:5][C:3]1=[O:4].O>Br>[CH3:1][N:2]1[C:12]2[C:7](=[C:8]([C:15](=[O:21])[CH2:16][NH:17][CH:18]([CH3:19])[CH3:20])[CH:9]=[CH:10][C:11]=2[OH:13])[CH:6]=[CH:5][C:3]1=[O:4]参加物
実験手順
2.0 g of 1-methyl-5-isopropylaminoacetyl-8-methoxycarbostyril (IIb) hydrochloride prepared as described in Example 3 was dissolved in 30 ml of a 47% aqueous solution of hydrobromic acid, and the solution was heated in an oil bath at a temperature of 120° to 130° C. for 8 hours under refluxing. 10 ml of water was then added to the reaction mixture followed by concentration by distillation. 10 ml of water was again added to the mixture followed by concentration. After allowing the mixture to cool, the precipitate formed was filtered and dissolved in 60 ml of water by heating. The resulting solution was adjusted to a pH of 6.5-7.5 with sodium bicarbonate and the precipitate formed was filtered. Recrystallization of the precipitate from ethanol yielded 0.45 g of white amorphous 1-methyl-5-isopropylaminoacetyl-8-hydroxycarbostyril (IIa) having a melting point of 136° to 138° C (with decomposition). The product thus obtained was confirmed by elemental analysis and IR and NMR spectral analyses.
後処理
- temperaturethe solution was heated in an oil bath at a temperature of 120° to 130° C. for 8 hours
- temperatureunder refluxing
- concentrationfollowed by concentration by distillation
- addition10 ml of water was again added to the mixture
- concentrationfollowed by concentration
- temperatureto cool
- customthe precipitate formed
- filtrationwas filtered
- dissolutiondissolved in 60 ml of water
- temperatureby heating
- customthe precipitate formed
- filtrationwas filtered
- customRecrystallization of the precipitate from ethanol
出典と根拠
- ORDレコード
- ord-5f482dfbc76644f88ef895b8f3fafef7
- 出典データセット
- uspto-grants-1977_05
- 特許番号
- US04022784
反応ノート
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