Sodium Hydroxide → 3-Amino-2-[1,1'-biphenyl]-4-yl-6,8-dichloro-4-quinolinecarboxylic acid
反応式
[Cl:1][C:2]1[CH:3]=[C:4]2[C:8](=[C:9]([Cl:11])[CH:10]=1)[NH:7][C:6](=[O:12])[C:5]2=O.[OH-:14].[Na+].Cl.[NH2:17][CH2:18][C:19]([C:21]1[CH:26]=[CH:25][C:24]([C:27]2[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=2)=[CH:23][CH:22]=1)=O>O.C(O)C.O.O1CCCC1>[NH2:17][C:18]1[C:19]([C:21]2[CH:26]=[CH:25][C:24]([C:27]3[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=3)=[CH:23][CH:22]=2)=[N:7][C:8]2[C:4]([C:5]=1[C:6]([OH:12])=[O:14])=[CH:3][C:2]([Cl:1])=[CH:10][C:9]=2[Cl:11]参加物
反応物 3
生成物 1
試薬・触媒・溶媒 3
反応条件
- 温度
- 90 °C
実験手順
A 3.02 g portion of 5,7-dichloroisatin was suspended in 25 ml of water in a 500 ml three-necked flask. A solution of 3.96 g of sodium hydroxide in 15 ml of water was added and the mixture heated to 90° C. A 6.0 g portion of 2-amino-4'-phenylacetophenone hydrochloride was dissolved in a mixture of 80 ml of absolute ethanol:water (1:1) and 20 ml of tetrahydrofuran. This solution was kept warm and with stirring, added dropwise to the 5,7-dichloroisatin solution over 1.5 hours. The resulting solution was refluxed 1.5 hours, then the solvent was distilled off at 85° C. The red solids were collected and washed with 50 ml of water. These solids were then stirred in 1800 ml of water, filtered and the filtrate acidified to pH 5 with glacial acetic acid. The resulting orange solids were collected and dried, giving 3.25 g of the desired product, mp 244°-245° C.
後処理
- temperatureThis solution was kept warm
- temperatureThe resulting solution was refluxed 1.5 hours
- distillationthe solvent was distilled off at 85° C
- customThe red solids were collected
- washwashed with 50 ml of water
- stirringThese solids were then stirred in 1800 ml of water
- filtrationfiltered
- customThe resulting orange solids were collected
- customdried
出典と根拠
- ORDレコード
- ord-4a06145db81d475e8aa07e4e275fb0b4
- 出典データセット
- uspto-grants-1990_11
- 特許番号
- US04968702
反応ノート
読み込み中…