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

HRID 1921280
ノート
印刷プレビュー

反応式

HRID 1921280 の反応式
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
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 962WaterHCID 7965CyclohexylamineHCID 13794930HCID 13794930、化合物

生成物 1

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

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

実験手順

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).

後処理

  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)

出典と根拠

ORDレコード
ord-497324d352824a2e924aa2e22acce240
出典データセット
uspto-grants-2012_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08173684B2

反応ノート

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