反応式
[NH2:1][C:2]1[C:7]([N+]([O-])=O)=[C:6]([CH3:11])[C:5]([N+:12]([O-])=O)=[CH:4][N:3]=1.[CH2:15]1[CH2:19]O[CH2:17][CH2:16]1.[C:20]([OH:26])(=O)[CH2:21][CH2:22][CH2:23][CH3:24].[NH4+:27].[OH-].[CH3:29]O>O.[Ni]>[O:26]=[C:20]([NH:27][C:16]1[CH:17]=[C:4]2[NH:3][C:2]([CH2:7][CH2:6][CH2:11][CH3:29])=[N:1][C:5]2=[N:12][C:15]=1[CH3:19])[CH2:21][CH2:22][CH2:23][CH3:24]参加物
反応条件
- 温度
- 80 °C
実験手順
A mixture of 2-amino-3,5-dinitro-4-methylpyridine (5.2 g, 26 mmol), THF (100 mL), methanol (1300 mL) and Raney-nickel (3 mL of a 1:1 suspension in H2O) was stirred under H2 (1 atm.) for 5 h. The mixture was quickly filtered into a flask containing 3 ml of conc. HCl and the solvent was removed in vacuo at r.t. To the resulting crude 2,3,5-triamino-6-methylpyridine HCl complex was added valeric acid (8.68 mL, 80 mmol) and polyphosphoric acid (100 mL) and this mixture was heated to 80° C. for 7 h. The warmed mixture was poured into stirred ice-H2O (500 mL) and this mixture was cooled and neutralized (to pH 3) by the addition of conc. NH4OH. Extraction with CH2Cl2 (5×50 mL), drying (Na2SO4), concentration and purification (SiO2, 5% MeOH/EtOAc) gave the title compound as a solid.
後処理
- filtrationThe mixture was quickly filtered into a flask
- additioncontaining 3 ml of conc. HCl
- customthe solvent was removed in vacuo at r.t
- additionThe warmed mixture was poured
- temperaturethis mixture was cooled
- extractionExtraction with CH2Cl2 (5×50 mL)
- customdrying
- concentration(Na2SO4), concentration and purification (SiO2, 5% MeOH/EtOAc)
出典と根拠
- ORDレコード
- ord-6de85dba48e842268fe764ab41bd33f6
- 出典データセット
- uspto-grants-1995_05
- 特許番号
- US05412097
関連ノート
読み込み中…