Acetic Acid → HCID 20145287、化合物
反応式
[C:1]([BH3-])#[N:2].[Na+].[C:5](O)(=O)C.N[C:10]1[CH:11]=[CH:12][C:13]([N:31]2[CH2:36][CH2:35][CH2:34][CH2:33][CH2:32]2)=[C:14]([CH:16]([CH:18]([C:28]([NH2:30])=[O:29])[C:19]2[CH:27]=[CH:26][C:22]([C:23]([OH:25])=[O:24])=[CH:21][CH:20]=2)[CH3:17])[CH:15]=1.C=O>C(#N)C.CN(C)C=O>[CH3:5][N:2]([CH3:1])[C:10]1[CH:11]=[CH:12][C:13]([N:31]2[CH2:36][CH2:35][CH2:34][CH2:33][CH2:32]2)=[C:14]([CH:16]([CH:18]([C:28]([NH2:30])=[O:29])[C:19]2[CH:27]=[CH:26][C:22]([C:23]([OH:25])=[O:24])=[CH:21][CH:20]=2)[CH3:17])[CH:15]=1参加物
実験手順
A tenth of a gram (1.589 m mol) of sodium cyanoborohydride and, after two minutes, 0.056 ml of glacial acetic acid were added at 20° C. to a stirred solution of 0.20 gm (0.5242 m mol) of 4-[(1-(5-amino-2-piperidino-phenyl)-ethyl)-aminocarbonylmethyl]-benzoic acid and 0.45 ml of 40% formalin in 2 ml of acetonitrile and 1 ml of absolute dimethyl formamide. After 1.5 hours the reaction mixture was evaporated in vacuo. The evaporation residue was dissolved in water by addition of hydrochloric acid at a pH of 2 to 3. After extraction with chloroform several times the aqueous phase was adjusted to a pH of 6 to 7 by means of saturated sodium bicarbonate solution and extracted several times with chloroform. This organic extract was dried and filtered. After evaporation in vacuo the evaporation residue was recrystallized from isopropanol. The colorless crystals were washed with absolute ether.
後処理
- customAfter 1.5 hours the reaction mixture was evaporated in vacuo
- dissolutionThe evaporation residue was dissolved in water by addition of hydrochloric acid at a pH of 2 to 3
- extractionAfter extraction with chloroform several times the aqueous phase
- extractionextracted several times with chloroform
- extractionThis organic extract
- customwas dried
- filtrationfiltered
- customAfter evaporation in vacuo the evaporation residue
- customwas recrystallized from isopropanol
- washThe colorless crystals were washed with absolute ether
出典と根拠
- ORDレコード
- ord-a68044cfcaed4a71b252f541f8e45ada
- 出典データセット
- uspto-grants-1988_04
- 特許番号
- US04735959
反応ノート
読み込み中…