4-Fluorobenzaldehyde → 3-Methyl 5-ethyl 1,4-dihydro-2,4-di-(4-fluorophenyl)-6-isopropylpyridine-3,5-di-carboxylate

HRID 365415ノート

反応式

HRID 365415 の反応式
[F:1][C:2]1[CH:9]=[CH:8][C:5]([CH:6]=O)=[CH:4][CH:3]=1.[F:10][C:11]1[CH:23]=[CH:22][C:14]([C:15]([CH2:17][C:18]([O:20][CH3:21])=[O:19])=O)=[CH:13][CH:12]=1.[NH2:24][C:25]([CH:32]([CH3:34])[CH3:33])=[CH:26][C:27]([O:29][CH2:30][CH3:31])=[O:28]>C(O)CO>[F:1][C:2]1[CH:9]=[CH:8][C:5]([C:6]2[NH:24][C:25]([CH:32]([CH3:33])[CH3:34])=[C:26]([C:27]([O:29][CH2:30][CH3:31])=[O:28])[CH:15]([C:14]3[CH:13]=[CH:12][C:11]([F:10])=[CH:23][CH:22]=3)[C:17]=2[C:18]([O:20][CH3:21])=[O:19])=[CH:4][CH:3]=1

参加物

5

実験手順

31 g (0.25 mol) of p-fluorobenzaldehyde, 49 g (0.25 mol) of methyl 4-fluorobenzoylacetate and 39.25 g (0.25 mol) of ethyl 3-amino-4-methyl-pent-2-enoate are boiled under reflux for 18 hours in 150 ml of ethylene glycol at a bath temperature of 130° C. The mixture is cooled to room temperature, extracted three times using 300 ml of diethyl ether, the combined ether phases are concentrated, and the residue is dissolved in 100 ml of toluene and chromatographed on 700 ml of silica gel (0.04-0.063 mm) using toluene as an eluent.

後処理

  1. extractionextracted three times
  2. concentrationthe combined ether phases are concentrated
  3. dissolutionthe residue is dissolved in 100 ml of toluene
  4. customchromatographed on 700 ml of silica gel (0.04-0.063 mm)

出典と根拠

ORDレコード
ord-bd915f11a9484b1ea6f258a9e7c239f8
出典データセット
uspto-grants-2000_10
特許番号
US06127383

反応ノート

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