反応式
CO[C:3]([C:5]1[N:6]=[CH:7][C:8]2[NH:9][C:10]3[C:15]([C:16]=2[CH:17]=1)=[CH:14][CH:13]=[CH:12][CH:11]=3)=[O:4].[CH3:18][NH2:19]>CO>[CH3:18][NH:19][C:3]([C:5]1[N:6]=[CH:7][C:8]2[NH:9][C:10]3[C:15]([C:16]=2[CH:17]=1)=[CH:14][CH:13]=[CH:12][CH:11]=3)=[O:4]参加物
4
実験手順
12 g of β-carbolin-3-carboxylic acid methyl ester is suspended in 130 ml of methanol; 130 ml of 40% aqueous methylamine is added thereto and the whole is boiled at reflux for 2 hours. After cooling, the mixture is suction-filtered. By extraction with 300 ml of hot methanol and crystallization from dimethylformamide/hexane, the β-carbolin-3-carboxylic acid N-methylamide of melting point 264°-266° C. is isolated from the filter residue in 43% yield.
後処理
- temperatureat reflux for 2 hours
- temperatureAfter cooling
- filtrationthe mixture is suction-filtered
- extractionBy extraction
- customwith 300 ml of hot methanol and crystallization from dimethylformamide/hexane
出典と根拠
- ORDレコード
- ord-1aa19bd488e4488f8303d7fac6287245
- 出典データセット
- uspto-grants-1991_04
- 特許番号
- US05010077
関連ノート
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