Benzyl Chloride → N2,N4,N4-trimethyl-N2-[1-(phenylmethyl)-4-piperidinyl]-2,4-pyrimidinediamine
反応式
Cl[CH2:2][C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1.[CH3:9][N:10]([CH:20]1[CH2:25][CH2:24][NH:23][CH2:22][CH2:21]1)[C:11]1[N:16]=[C:15]([N:17]([CH3:19])[CH3:18])[CH:14]=[CH:13][N:12]=1.C(N(CC)CC)C>CN(C)C(=O)C>[CH3:9][N:10]([CH:20]1[CH2:25][CH2:24][N:23]([CH2:2][C:3]2[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=2)[CH2:22][CH2:21]1)[C:11]1[N:16]=[C:15]([N:17]([CH3:18])[CH3:19])[CH:14]=[CH:13][N:12]=1参加物
5
反応条件
- 温度
- 75 °C
実験手順
A mixture of chloromethylbenzene (1.9 g), intermediate 2 (3 g) and triethylamine (2.62 g) in N,N-dimethylacetamide (55 ml) was stirred for 2 hours at 75° C. The reaction mixture was poured out into ice-water and extracted with toluene. The separated organic layer was washed three times with water, dried, filtered and the solvent evaporated. The residue was dissolved in boiling petroleum ether and treated with activated charcoal. The mixture was filtered warm over dicalite, and the filtrate was concentrated. The concentrate was cooled on an ice-bath and the resulting precipitate was filtered off and dried, yielding 2.3 g (54.4%) of N2,N4,N4-trimethyl-N2-[1-(phenylmethyl)-4-piperidinyl]-2,4-pyrimidinediamine (comp. 8).
後処理
- extractionextracted with toluene
- washThe separated organic layer was washed three times with water
- customdried
- filtrationfiltered
- customthe solvent evaporated
- dissolutionThe residue was dissolved
- additiontreated with activated charcoal
- filtrationThe mixture was filtered
- temperaturewarm over dicalite
- concentrationthe filtrate was concentrated
- temperatureThe concentrate was cooled on an ice-bath
- filtrationthe resulting precipitate was filtered off
- customdried
出典と根拠
- ORDレコード
- ord-39e5f7c0c7a04a6b8f610113f81985dc
- 出典データセット
- uspto-grants-2002_05
- 特許番号
- US06395742B1
反応ノート
読み込み中…