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

HRID 255664
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HRID 255664 반응식
[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
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참가 물질

3

반응물 1

HCID 178500768HCID 178500768, 화합물

생성물 1

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

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-552443bc5acc454599975342a96f610b
출처 데이터셋
uspto-grants-1987_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04698352

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