Diethyl Oxalate → HCID 12802779、化合物

HRID 1448827ノート

反応式

HRID 1448827 の反応式
[Cl:1][C:2]1[CH:3]=[C:4]([CH:20]=[CH:21][C:22]=1[Cl:23])[CH2:5][N:6]1[C:15]2[C:10](=[CH:11][C:12]([F:17])=[C:13]([F:16])[CH:14]=2)[C:9]([CH3:18])=[CH:8][C:7]1=[O:19].C(OCC)(=O)[C:25]([O:27]CC)=[O:26].[O-]CC.[K+]>C1C=CC=CC=1.C(O)C>[Cl:1][C:2]1[CH:3]=[C:4]([CH:20]=[CH:21][C:22]=1[Cl:23])[CH2:5][N:6]1[C:15]2[C:10](=[CH:11][C:12]([F:17])=[C:13]([F:16])[CH:14]=2)[C:9]([CH2:18][C:25]([OH:27])=[O:26])=[CH:8][C:7]1=[O:19]

参加物

6

反応物 3

HCID 7268Diethyl OxalateHCID 203756291-[(3,4-Dichlorophenyl)methyl]-6,7-difluoro-4-methylquinolin-2(1H)-oneHCID 23670592Potassium ethoxide

生成物 1

HCID 12802779HCID 12802779、化合物収率 10%

試薬・触媒・溶媒 2

HCID 241Benzene溶媒2 回HCID 702Ethanol溶媒

反応条件

温度
50 °C

実験手順

A solution of 1-(3,4-dichlorobenzyl)-6,7-difluoro-1,2-dihydro-4-methyl-2-oxoquinoline (5 g.) in benzene (15 ml.) was added with stirring at ambient temperature to a mixture of diethyl oxalate (2.3 g.), benzene (2 ml.) and a 6 N-solution of potassium ethoxide in ethanol (6 ml.). The mixture was allowed to stand overnight at ambient temperature under dry nitrogen. The yellow solid was filtered off, washed with benzene (5 ml.) and dried by suction on the filter. The dried solid (5.7 g.) was mixed with 2.77 N-aqueous sodium hydroxide (21 ml.) at 0° C. and kept at 0° C. overnight. Ice (11.5 g.) and then 100 vol. hydrogen peroxide (4.04 ml.) were added to the mixture and it was again kept overnight at 0° C. A further quantity of 100 vol. hydrogen peroxide (1.7 ml.) was added and the mixture kept at 0° C. for 72 hours. The mixture was then treated with manganese dioxide (1 g.). When the effervescence had ceased the mixture was warmed to 50° C. and filtered. The filter cake was washed with warm 2.77 N-aqueous sodium hydroxide (20 ml.) and the total filtrate acidified with concentrated hydrochloric acid. The precipitate was collected and recrystallised first from a mixture (1/2 v/v) of ethyl acetate and cyclohexane, and then from ethanol to give 1-(3,4-dichlorobenzyl)-6,7-difluoro-1,2-dihydro-2-oxoquinol-4-ylacetic acid m.p. 185°-7° C. (dec.), in 10% yield.

後処理

  1. filtrationThe yellow solid was filtered off
  2. washwashed with benzene (5 ml.)
  3. customdried by suction on the filter
  4. additionThe dried solid (5.7 g.) was mixed with 2.77 N-aqueous sodium hydroxide (21 ml.) at 0° C.
  5. waitkept at 0° C. overnight
  6. additionIce (11.5 g.) and then 100 vol. hydrogen peroxide (4.04 ml.) were added to the mixture and it
  7. waitwas again kept overnight at 0° C
  8. additionA further quantity of 100 vol. hydrogen peroxide (1.7 ml.) was added
  9. waitthe mixture kept at 0° C. for 72 hours
  10. additionThe mixture was then treated with manganese dioxide (1 g.)
  11. filtrationfiltered
  12. washThe filter cake was washed
  13. temperaturewith warm 2.77 N-aqueous sodium hydroxide (20 ml.)
  14. customThe precipitate was collected
  15. customrecrystallised first from a mixture (1/2 v/v) of ethyl acetate and cyclohexane

出典と根拠

ORDレコード
ord-a810c78cfa5045708455adcfc23965e3
出典データセット
uspto-grants-1980_02
特許番号
US04187310

反応ノート

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