Acetic acid, 2-(triphenylphosphoranylidene)-, ethyl ester → HCID 19842246、化合物

HRID 1638341

反応式

HRID 1638341 の反応式
[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([N:8]2[C:16](=O)[C:15]3[C:10](=[N:11][CH:12]=[CH:13][N:14]=3)[CH:9]2[OH:18])=[N:6][CH:7]=1.[CH2:19]([O:21][C:22]([CH:24]=P(C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1)=[O:23])[CH3:20]>C1(C)C=CC=CC=1>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([N:8]2[C:9](=[O:18])[C:10]3[C:15](=[N:14][CH:13]=[CH:12][N:11]=3)[CH:16]2[CH2:24][C:22]([O:21][CH2:19][CH3:20])=[O:23])=[N:6][CH:7]=1

参加物

4

反応物 2

HCID 70670Acetic acid, 2-(triphenylphosphoranylidene)-, ethyl esterHCID 64519726-(5-Chloro-2-pyridyl)-6,7-dihydro-7-hydroxy-5H-pyrrolo(3,4-b)pyrazin-5-one

生成物 1

HCID 19842246HCID 19842246、化合物収率 90.4%

試薬・触媒・溶媒 1

HCID 1140Toluene溶媒

実験手順

6-(5-Chloro-2-pyridyl)-6,7-dihydro-7-hydroxy-5H-pyrrolo[3,4-b]pyrazin-5-one (1.05 g) and ethoxycarbonylmethylenetriphenylphosphorane (1.39 g) were dissolved in dry toluene (30 ml) and the solution was refluxed for 6 hours. After cooling, the solvent was distilled off and the residue was purified by silica gel column chromatography. Fractions eluted with dichloromethaneethyl acetate (2:1) were collected and the solvent was distilled off to give crude crystals. Recrystallization from ether-dichloromethane (5:1) gave 1.2 g of 6-(5-chloropyridyl)-6,7-dihydro-7-ethoxycarbonylmethyl-5H-pyrrolo[3,4-b]pyrazin-5-one.

後処理

  1. temperaturethe solution was refluxed for 6 hours
  2. temperatureAfter cooling
  3. distillationthe solvent was distilled off
  4. customthe residue was purified by silica gel column chromatography
  5. washFractions eluted with dichloromethaneethyl acetate (2:1)
  6. customwere collected
  7. distillationthe solvent was distilled off
  8. customto give crude crystals
  9. customRecrystallization from ether-dichloromethane (5:1)

出典と根拠

ORDレコード
ord-cc2ffdd26b5e4c0da7999f97296c7bce
出典データセット
uspto-grants-1989_11
特許番号
US04879293

関連ノート

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