Hydrochloric Acid → HCID 178428133、化合物
反応式
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([F:8])=[CH:4][C:3]=1[CH:9]1[CH2:18][C:17]2[N:16]=[CH:15][CH:14]=[C:13]([CH3:19])[C:12]=2[C:11](=O)[CH2:10]1.[C:21]([NH:24][NH2:25])([NH2:23])=[NH:22].Cl.Cl.O>C(O)C>[ClH:1].[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([F:8])=[CH:4][C:3]=1[CH:9]1[CH2:18][C:17]2[N:16]=[CH:15][CH:14]=[C:13]([CH3:19])[C:12]=2[C:11](=[N:25][NH:24][C:21]([NH2:23])=[NH:22])[CH2:10]1参加物
実験手順
A solution of 7-(2-chloro-5-fluorophenyl)-4-methyl-5,6,7,8-tetrahydroquinolin-5-one in ethanol (10 ml) was combined with aminoguanidine hydrochloride (0.041 g), concentrated hydrochloric acid (0.078 ml) and water (0.078 ml), and the mixture was heated under reflux for 4 hours. The solvent was distilled off under reduced pressure, and the residue was combined with water and the aqueous layer was washed with ethyl acetate. The aqueous layer was made alkaline with aqueous sodium hydrogen carbonate and extracted with ethyl acetate. The organic layer was washed successively with water and saturated brine, dried over magnesium sulfate and concentrated under reduced pressure. The residue was dissolved in 1N hydrochloric acid (1 ml) and concentrated. The resultant crystal was recrystallized from ethanol-ethyl acetate to obtain 7-(2-chloro-5-fluorophenyl)-5-guanidinoimino-4-methyl-5,6,7,8-tetrahydroquinoline hydrochloride (Compound G) (0.05 g) as a colorless crystal.
後処理
- temperaturethe mixture was heated
- temperatureunder reflux for 4 hours
- distillationThe solvent was distilled off under reduced pressure
- washthe aqueous layer was washed with ethyl acetate
- extractionextracted with ethyl acetate
- washThe organic layer was washed successively with water and saturated brine
- dry with materialdried over magnesium sulfate
- concentrationconcentrated under reduced pressure
- dissolutionThe residue was dissolved in 1N hydrochloric acid (1 ml)
- concentrationconcentrated
- customThe resultant crystal was recrystallized from ethanol-ethyl acetate
出典と根拠
- ORDレコード
- ord-95fab42f68de4fb9a9a1fcd6b5d81751
- 出典データセット
- uspto-grants-2004_03
- 特許番号
- US06706732B1
反応ノート
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