反応式
[CH3:1][C:2]([CH2:4][CH2:5][C:6]([OH:8])=[O:7])=[O:3].Cl.[Cl:10][C:11]1[CH:20]=[C:19]2[C:14]([C:15]([N:21]([C:25]3[CH:30]=[CH:29][C:28]([O:31][CH3:32])=[CH:27][CH:26]=3)N=CC)=[N:16][CH:17]=[N:18]2)=[CH:13][CH:12]=1>O>[OH2:3].[CH3:1][C:2]1[N:21]([C:15]2[C:14]3[C:19](=[CH:20][C:11]([Cl:10])=[CH:12][CH:13]=3)[N:18]=[CH:17][N:16]=2)[C:25]2[C:26]([C:4]=1[CH2:5][C:6]([OH:8])=[O:7])=[CH:27][C:28]([O:31][CH3:32])=[CH:29][CH:30]=2参加物
実験手順
A mixture of laevulinic acid (15g.) and acetaldehyde N1 -(7-chloroquinazolin-4-yl)-p-methoxyphenylhydrazone hydrochloride (3.3g.) was heated at 95°-100° C. for 18 hours. The mixture was poured into water (ca 300ml.), and the precipitated pale yellow solid was collected by filtration and dissolved in a mixture of water (80ml.) and ammonia solution (specific gravity 0.88, ca 5ml.). The solution was washed with ethyl acetate (2 × 25ml.). Addition of sodium chloride (ca 10g.) to the aqueous phase caused a yellow solid to precipitate. This was collected by filtration, and then dissolved in water. The solution was acidified with glacial acetic acid until precipitation was complete. The mixture was filtered to give, as solid residue, 2-methyl-5-methoxy-1-(7-chloroquinazolin-4-yl)indol-3-ylacetic acid monohydrate, m.p. 98°-100° C.
後処理
- temperaturewas heated at 95°-100° C. for 18 hours
- filtrationthe precipitated pale yellow solid was collected by filtration
- dissolutiondissolved in a mixture of water (80ml.) and ammonia solution (specific gravity 0.88, ca 5ml.)
- washThe solution was washed with ethyl acetate (2 × 25ml.)
- additionAddition of sodium chloride (ca 10g.) to the aqueous phase
- customto precipitate
- filtrationThis was collected by filtration
- dissolutiondissolved in water
- customThe solution was acidified with glacial acetic acid until precipitation
- filtrationThe mixture was filtered
出典と根拠
- ORDレコード
- ord-157e2c242f784cbaac7562b73481385d
- 出典データセット
- uspto-grants-1977_03
- 特許番号
- US04012513
関連ノート
読み込み中…