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HCID 178500768、化合物 → Methyl 6-(cyclohexen-4-yl)-1-(4-hydroxyphenyl)-4-oxo-1,4,5,6-tetrahydronicotinate

HRID 255664
ノート
印刷プレビュー

反応式

HRID 255664 の反応式
[CH:1]1[CH2:6][CH2:5][CH:4]([CH:7]=[CH:8][C:9](=[O:24])[C:10](=[CH:15][NH:16][C:17]2[CH:22]=[CH:21][C:20]([OH:23])=[CH:19][CH:18]=2)[C:11]([O:13][CH3:14])=[O:12])[CH2:3][CH:2]=1>CN(C)C=O>[CH:1]1[CH2:6][CH2:5][CH:4]([CH:7]2[CH2:8][C:9](=[O:24])[C:10]([C:11]([O:13][CH3:14])=[O:12])=[CH:15][N:16]2[C:17]2[CH:22]=[CH:21][C:20]([OH:23])=[CH:19][CH:18]=2)[CH2:3][CH:2]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

3

反応物 1

HCID 178500768HCID 178500768、化合物

生成物 1

HCID 14010724Methyl 6-(cyclohexen-4-yl)-1-(4-hydroxyphenyl)-4-oxo-1,4,5,6-tetrahydronicotinate収率 70%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

実験手順

In 20 ml of N,N-dimethylformamide was dissolved 2.0 g of methyl 5-(cyclohexen-4-yl)-2-(4-hydroxyphenylaminomethylene)-3-oxo-4-pentenoate, and they were reacted at 140° C. for 4 hours. After completion of the reaction, the solvent was removed by distillation under reduced pressure, and to the residue was added 50 ml of dioxane, after which the precipitated crystals were collected by filtration and washed with 30 ml of diethyl ether to obtain 1.4 g of methyl 6-(cyclohexen-4-yl)-1-(4-hydroxyphenyl)-4-oxo-1,4,5,6-tetrahydronicotinate having a melting point of 155°-157° C.

後処理

  1. customwere reacted at 140° C. for 4 hours
  2. customAfter completion of the reaction
  3. customthe solvent was removed by distillation under reduced pressure
  4. additionto the residue was added 50 ml of dioxane
  5. filtrationafter which the precipitated crystals were collected by filtration
  6. washwashed with 30 ml of diethyl ether

出典と根拠

ORDレコード
ord-552443bc5acc454599975342a96f610b
出典データセット
uspto-grants-1987_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04698352

反応ノート

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