Ethanol → 2-Phthalimidomethyl-6-methyl-4-(-pyridyl)-1,4-dihydropyridine-3,5-dicarboxylic acid diethyl ester

HRID 1449011

Reaktionsgleichung

Reaktionsgleichung von HRID 1449011
[N:1]1[CH:6]=[CH:5][CH:4]=[C:3](C=O)[CH:2]=1.[CH2:9]([O:11][C:12](=[O:28])[CH2:13][C:14]([CH2:16][N:17]1[C:21](=[O:22])[C:20]2=[CH:23][CH:24]=[CH:25][CH:26]=[C:19]2[C:18]1=[O:27])=O)[CH3:10].[CH2:29]([O:31][C:32](=[O:37])/[CH:33]=[C:34](\[NH2:36])/[CH3:35])[CH3:30].[CH2:38](O)C>>[CH2:9]([O:11][C:12]([C:13]1[CH:38]([C:6]2[CH:5]=[CH:4][CH:3]=[CH:2][N:1]=2)[C:33]([C:32]([O:31][CH2:29][CH3:30])=[O:37])=[C:34]([CH3:35])[NH:36][C:14]=1[CH2:16][N:17]1[C:21](=[O:22])[C:20]2=[CH:23][CH:24]=[CH:25][CH:26]=[C:19]2[C:18]1=[O:27])=[O:28])[CH3:10]

Komponenten

5

Versuchsvorschrift

A solution of 4.7 ccs of pyridine-3-aldehyde, 12.4 g of phthalimidoacetoacetic acid ethyl ester and 5.85 g of β-aminocrotonic acid ethyl ester in 100 ccs of ethanol is heated under reflux for 24 hours and, after cooling and filtering, crystals (beige) of melting point 165° C. are obtained, yield: 65%.

Aufarbeitung

  1. temperatureunder reflux for 24 hours
  2. temperatureafter cooling
  3. filtrationfiltering
  4. customcrystals (beige) of melting point 165° C. are obtained

Quellen und Nachweise

ORD-Eintrag
ord-37f2c0327a4a4334b7309a293b2b0a7c
Quelldatensatz
uspto-grants-1980_02
Patentnummer
US04188395

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