反応式
[NH2:1][C@@H:2]([C:13]([OH:15])=[O:14])[CH2:3][C:4]1[C:12]2[C:7](=[CH:8][CH:9]=[CH:10][CH:11]=2)[NH:6][CH:5]=1.[OH-].[Na+].[CH2:18]=O.Cl>O>[CH2:18]1[C:5]2[NH:6][C:7]3[C:12]([C:4]=2[CH2:3][C@H:2]([C:13]([OH:15])=[O:14])[NH:1]1)=[CH:11][CH:10]=[CH:9][CH:8]=3参加物
6
実験手順
20.0 g D-tryptophan is suspended in 40 ml of water and 7.83 g 50%(w/w) sodium hydroxide solution is added and this mixture is stirred to give a clear solution. 7.95 g 37% formaldehyde is added and this mixture is stirred for 2 hours at room temperature, then refluxed for 3 hours. The hot solution is poured into 200 ml water and, with vigorous stirring, the pH is adjust to 5 with 6N hydrochloric acid, giving a precipitate. The slurry is stirred for 18 hours, filtered, and the solid dried at 70° C./0.1 mm Hg overnight to give 18.5 g (3R)-1,2,3,4-tetrahydro-9H-pyrido[3,4-b]indole-3-carboxylic acid.
後処理
- customto give a clear solution
- stirringthis mixture is stirred for 2 hours at room temperature
- temperaturerefluxed for 3 hours
- customgiving a precipitate
- stirringThe slurry is stirred for 18 hours
- filtrationfiltered
- customthe solid dried at 70° C./0.1 mm Hg overnight
出典と根拠
- ORDレコード
- ord-265860efbbbd464a9f4f85ffc7463a62
- 出典データセット
- uspto-grants-1992_11
- 特許番号
- US05162336
関連ノート
読み込み中…