Benzyl Chloride → N2,N4,N4-trimethyl-N2-[1-(phenylmethyl)-4-piperidinyl]-2,4-pyrimidinediamine

HRID 1937415ノート

反応式

HRID 1937415 の反応式
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

  1. extractionextracted with toluene
  2. washThe separated organic layer was washed three times with water
  3. customdried
  4. filtrationfiltered
  5. customthe solvent evaporated
  6. dissolutionThe residue was dissolved
  7. additiontreated with activated charcoal
  8. filtrationThe mixture was filtered
  9. temperaturewarm over dicalite
  10. concentrationthe filtrate was concentrated
  11. temperatureThe concentrate was cooled on an ice-bath
  12. filtrationthe resulting precipitate was filtered off
  13. 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

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