Phosphorus oxychloride → 1-(2-benzoyloxyethyl)-4-chloro-1H-imidazo[4,5-c]quinoline

HRID 255519ノート

反応式

HRID 255519 の反応式
[C:1]([O:9][CH2:10][CH2:11][N:12]1[C:24]2[C:23]3[CH:22]=[CH:21][CH:20]=[CH:19][C:18]=3[N+:17]([O-])=[CH:16][C:15]=2[N:14]=[CH:13]1)(=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.P(Cl)(Cl)([Cl:28])=O>>[C:1]([O:9][CH2:10][CH2:11][N:12]1[C:24]2[C:23]3[CH:22]=[CH:21][CH:20]=[CH:19][C:18]=3[N:17]=[C:16]([Cl:28])[C:15]=2[N:14]=[CH:13]1)(=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1

参加物

3

実験手順

A mixture of 50 g (0.15 mole) of 1-(2-benzoyloxyethyl)-1H-imidazo[4,5-c]quinolin-5-oxide (from Example 119) and 200 ml of phosphorus oxychloride was heated for two hours on a steam bath. The mixture was then partially evaporated in vacuo. The mixture was then poured over ice and the solution was neutralized with sodium hydroxide. The product was separated by filtration, dissolved in dichloromethane, and the solution was washed with aqueous sodium bicarbonate solution and then dried. Evaporation provided a solid which was recrystallized from a 50:50 methanol:dichloromethane solution to provide white 1-(2-benzoyloxyethyl)-4-chloro-1H-imidazo[4,5-c]quinoline, m.p. 186°-190° C. Analysis: Calculated for C19H14ClN3O2 : %C, 64.9; %H, 4.0; %N, 12.0; Found: %C, 64.8; %H, 3.8; %N, 12.1.

後処理

  1. temperaturewas heated for two hours on a steam bath
  2. customThe mixture was then partially evaporated in vacuo
  3. additionThe mixture was then poured over ice
  4. customThe product was separated by filtration
  5. dissolutiondissolved in dichloromethane
  6. washthe solution was washed with aqueous sodium bicarbonate solution
  7. customdried
  8. customEvaporation
  9. customprovided a solid which
  10. customwas recrystallized from a 50:50 methanol

出典と根拠

ORDレコード
ord-1e36455ef6a74e46a3d22c9357546890
出典データセット
uspto-grants-1987_10
特許番号
US04698348

反応ノート

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