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

HRID 1789418ノート

反応式

HRID 1789418 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 50g (0.15 mole) of 1-(2-benzoyloxyethyl)-1H-imidazo[4,5-c]quinolin-5-oxide (from Example 116) 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 poured over ice, and the solution was neutralized with sodium hydroxide. The product was separated by filtration and dissolved in dichloromethane, and the solution was washed with aqueous sodium bicarbonate solution and 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 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-fd07e5c4703549e79fcc07e18a5b58b2
出典データセット
uspto-grants-1987_08
特許番号
US04689338

反応ノート

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