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Water → Methyl 1-cyclohexyl-6-oxo-1,6-dihydro-3-pyridinecarboxylate

HRID 1921280
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HRID 1921280 반응식
CO/[CH:3]=[C:4](\[C:11]([O:13][CH3:14])=[O:12])/[CH:5]=[CH:6]/[C:7]([O:9]C)=O.[CH:15]1([NH2:21])[CH2:20][CH2:19][CH2:18][CH2:17][CH2:16]1.O>CN(C=O)C>[CH:15]1([N:21]2[C:7](=[O:9])[CH:6]=[CH:5][C:4]([C:11]([O:13][CH3:14])=[O:12])=[CH:3]2)[CH2:20][CH2:19][CH2:18][CH2:17][CH2:16]1
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참가 물질

5

반응물 3

HCID 962WaterHCID 7965CyclohexylamineHCID 13794930HCID 13794930, 화합물

생성물 1

HCID 15946190Methyl 1-cyclohexyl-6-oxo-1,6-dihydro-3-pyridinecarboxylate수율 36%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

To a solution of dimethyl (2E,4Z)-4-(methoxymethylene)-2-pentenedioate (1.23 g) in DMF (30 mL) was added cyclohexanamine (670 mg) at 0° C., and the mixture was stirred at the same temperature for 30 min under a nitrogen atmosphere. The reaction mixture was heated to reflux for 5 hr. The mixture was cooled with an ice-water bath and poured into water (100 mL). The resulted mixture was extracted with EtOAc (100 mL×2), and the organic phases were combined, washed with brine two times, dried over MgSO4, filtered and evaporated in vacuo. The residue was purified by silica gel column chromatography eluting with EtOAc-hexane (1:2-1:1) to give methyl 1-cyclohexyl-6-oxo-1,6-dihydro-3-pyridinecarboxylate (520 mg).

후처리

  1. temperatureThe reaction mixture was heated
  2. temperatureto reflux for 5 hr
  3. temperatureThe mixture was cooled with an ice-water bath
  4. extractionThe resulted mixture was extracted with EtOAc (100 mL×2)
  5. washwashed with brine two times
  6. dry with materialdried over MgSO4
  7. filtrationfiltered
  8. customevaporated in vacuo
  9. customThe residue was purified by silica gel column chromatography
  10. washeluting with EtOAc-hexane (1:2-1:1)

출처 및 근거

ORD 기록
ord-497324d352824a2e924aa2e22acce240
출처 데이터셋
uspto-grants-2012_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08173684B2

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