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

HRID 4667

반응식

HRID 4667 반응식
[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]([CH2:28][CH3:29])=[C:17]1[C:30]([O:32][CH2:33][CH3:34])=[O:31].[C:35]1([O:41][CH2:42][CH:43]2[O:45][CH2:44]2)[CH:40]=[CH:39][CH:38]=[CH:37][CH:36]=1>CO>[CH2:28]([C:18]1[NH:19][C:20]([CH3:27])=[C:21]([C:22]([O:24][CH2:25][CH3:26])=[O:23])[CH:16]([C:8]2[CH:9]=[C:10]([N+:13]([O-:15])=[O:14])[CH:11]=[CH:12][C:7]=2[O:6][CH2:5][CH2:4][CH2:3][CH2:2][NH:1][CH2:44][CH:43]([OH:45])[CH2:42][O:41][C:35]2[CH:40]=[CH:39][CH:38]=[CH:37][CH:36]=2)[C:17]=1[C:30]([O:32][CH2:33][CH3:34])=[O:31])[CH3:29]

참가 물질

4

실험 절차

In 46 ml of methanol were dissolved 4.62 g of diethyl 4-[2-(4-aminobutoxy)-5-nitrophenyl]-2-ethyl-6-methyl-1,4-dihydropyridine-3,5-dicarboxylate and 1.46 g of glycidyl phenyl ether, and the solution formed was refluxed under heating for 15 hours. After cooling the reaction solution, the solution was concentrated under reduced pressure. The residue was subjected to silica gel column chromatography, and the product was eluted with chloroform-methanol (95:5 v/v). Crude crystals were recrystallized from ethanol to give 1.22 g of diethyl 2-ethyl-4-[2-[4-(2-hydroxy-3-phenoxypropylamino)butoxy]-5-nitrophenyl]-6-methyl-1,4-dihydropyridine-3,5-dicarboxylate.

후처리

  1. customthe solution formed
  2. temperaturewas refluxed
  3. temperatureunder heating for 15 hours
  4. temperatureAfter cooling the reaction solution
  5. concentrationthe solution was concentrated under reduced pressure
  6. washthe product was eluted with chloroform-methanol (95:5 v/v)
  7. customCrude crystals were recrystallized from ethanol

출처 및 근거

ORD 기록
ord-2f3c02f79686496e8840329c81d3621d
출처 데이터셋
uspto-grants-1988_02
특허 번호
US04727082

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