Phenyl glycidyl ether → Diethyl 4-[2-[4-(2-hydroxy-3-phenoxypropylamino)butoxy]-5-nitrophenyl]-2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate

HRID 4664

反応式

HRID 4664 の反応式
[NH2:1][CH2:2][CH2:3][CH2:4][CH2:5][O:6][C:7]1[CH:12]=[CH:11][C:10]([N+:13]([O-:15])=[O:14])=[CH:9][C:8]=1[CH:16]1[C:21]([C:22]([O:24][CH2:25][CH3:26])=[O:23])=[C:20]([CH3:27])[NH:19][C:18]([CH3:28])=[C:17]1[C:29]([O:31][CH2:32][CH3:33])=[O:30].[C:34]1([O:40][CH2:41][CH:42]2[O:44][CH2:43]2)[CH:39]=[CH:38][CH:37]=[CH:36][CH:35]=1>CO>[OH:44][CH:42]([CH2:41][O:40][C:34]1[CH:39]=[CH:38][CH:37]=[CH:36][CH:35]=1)[CH2:43][NH:1][CH2:2][CH2:3][CH2:4][CH2:5][O:6][C:7]1[CH:12]=[CH:11][C:10]([N+:13]([O-:15])=[O:14])=[CH:9][C:8]=1[CH:16]1[C:21]([C:22]([O:24][CH2:25][CH3:26])=[O:23])=[C:20]([CH3:27])[NH:19][C:18]([CH3:28])=[C:17]1[C:29]([O:31][CH2:32][CH3:33])=[O:30]

参加物

4

実験手順

In 500 ml of methanol were dissolved 5.2 g of diethyl 4-[2-(4-aminobutoxy)-5-nitrophenyl]-2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate and 1.7 g of glycidyl phenyl ether, and the solution thus formed was refluxed under heating for 16 hours. The solvent was distilled off under reduced pressure. The residue was subjected to silica gel column chromatography, and the product was eluted with chlroform-methanol (95:5 v/v). Crude crystals were recrystallized from ethanol to give 2.2 g of diethyl 4-[2-[4-(2-hydroxy-3-phenoxypropylamino)butoxy]-5-nitrophenyl]-2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate.

後処理

  1. customthe solution thus formed
  2. temperaturewas refluxed
  3. temperatureunder heating for 16 hours
  4. distillationThe solvent was distilled off under reduced pressure
  5. washthe product was eluted with chlroform-methanol (95:5 v/v)
  6. customCrude crystals were recrystallized from ethanol

出典と根拠

ORDレコード
ord-f7d6b5a0a92348dbad2bb63286d5a2ea
出典データセット
uspto-grants-1988_02
特許番号
US04727082

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