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Sodium Carbonate → 6-(2,4-Difluorophenyl)-5-(4-formylphenyl)-pyrazolo[1,5-a]pyrimidine-3-carboxylic acid methyl ester

HRID 1851236
ノート
印刷プレビュー

反応式

HRID 1851236 の反応式
[CH3:1][O:2][C:3]([C:5]1[CH:6]=[N:7][N:8]2[CH:13]=[C:12]([C:14]3[CH:19]=[CH:18][C:17]([F:20])=[CH:16][C:15]=3[F:21])[C:11](Cl)=[N:10][C:9]=12)=[O:4].C([O-])([O-])=O.[Na+].[Na+].[CH:29]([C:31]1[CH:36]=[CH:35][C:34](B(O)O)=[CH:33][CH:32]=1)=[O:30]>C(COC)OC.C1C=CC(P(C2C=CC=CC=2)[C-]2C=CC=C2)=CC=1.C1C=CC(P(C2C=CC=CC=2)[C-]2C=CC=C2)=CC=1.Cl[Pd]Cl.[Fe+2]>[CH3:1][O:2][C:3]([C:5]1[CH:6]=[N:7][N:8]2[CH:13]=[C:12]([C:14]3[CH:19]=[CH:18][C:17]([F:20])=[CH:16][C:15]=3[F:21])[C:11]([C:34]3[CH:35]=[CH:36][C:31]([CH:29]=[O:30])=[CH:32][CH:33]=3)=[N:10][C:9]=12)=[O:4]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 10340Sodium CarbonateHCID 5910734-Formylphenylboronic AcidHCID 867030475-Chloro-6-(2,4-difluorophenyl)pyrazolo[1,5-a]pyrimidine-3-carboxylic acid methyl ester

生成物 1

HCID 867030506-(2,4-Difluorophenyl)-5-(4-formylphenyl)-pyrazolo[1,5-a]pyrimidine-3-carboxylic acid methyl ester収率 44.1%

試薬・触媒・溶媒 2

HCID 44119782
Bis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)
触媒
HCID 80711,2-Dimethoxyethane溶媒

反応条件

温度
90 °C

実験手順

130 mg (0.4 mmol) 5-Chloro-6-(2,4-difluorophenyl)pyrazolo[1,5-a]pyrimidine-3-carboxylic acid methyl ester are given in 1.4 mL dimethoxyethane (no complete dissolution). 0.8 mL Na2CO3 solution (10%) and 66 mg (0.44 mmol) 4-formylphenylboronic acid are added. After addition of 15 mg (0.02 mmol) 1,1′-bis(diphenylphosphino)ferrocenedichloropalladium(II) the reaction mixture is purged 3× with argon and heated at 90° C. for 18 hours (complete dissolution). The reaction mixture is cooled down, treated with water and diluted with dichloromethane. The water phase is extracted once more with dichloromethane and the combined organic phases are washed with brine and dried (Na2SO4). The solvent is removed and the crude product purified via chromatography (silicagel, dichloromethane/methanol). 69.4 mg (41.7%) of the desired aldehyde are obtained.

後処理

  1. dissolutionno complete dissolution)
  2. customis purged 3× with argon
  3. dissolution(complete dissolution)
  4. temperatureThe reaction mixture is cooled down
  5. additiontreated with water
  6. additiondiluted with dichloromethane
  7. extractionThe water phase is extracted once more with dichloromethane
  8. washthe combined organic phases are washed with brine
  9. dry with materialdried (Na2SO4)
  10. customThe solvent is removed
  11. customthe crude product purified via chromatography (silicagel, dichloromethane/methanol)

出典と根拠

ORDレコード
ord-971397b350fa443595a0095753c0b991
出典データセット
uspto-grants-2015_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08957064B2

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート