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Sodium Carbonate → 4-(2-Methyl-6-phenyl-imidazo[1,2-a]pyrimidin-7-yl)benzaldehyde

HRID 1851187
ノート
印刷プレビュー

反応式

HRID 1851187 の反応式
Cl[C:2]1[C:7]([C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=2)=[CH:6][N:5]2[CH:14]=[C:15]([CH3:17])[N:16]=[C:4]2[N:3]=1.C([O-])([O-])=O.[Na+].[Na+].[CH:24]([C:26]1[CH:31]=[CH:30][C:29](B(O)O)=[CH:28][CH:27]=1)=[O:25]>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]>[CH3:17][C:15]1[N:16]=[C:4]2[N:3]=[C:2]([C:29]3[CH:30]=[CH:31][C:26]([CH:24]=[O:25])=[CH:27][CH:28]=3)[C:7]([C:8]3[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=3)=[CH:6][N:5]2[CH:14]=1
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 866903007-Chloro-2-methyl-6-phenyl-imidazo[1,2-a]pyrimidine

生成物 1

HCID 867030344-(2-Methyl-6-phenyl-imidazo[1,2-a]pyrimidin-7-yl)benzaldehyde

試薬・触媒・溶媒 2

HCID 44119782Bis(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

2.3 g (9.4 mmol) 7-Chloro-2-methyl 6-phenyl-imidazo[1,2-a]pyrimidine is given in 32 mL dimethoxyethane (not completely dissolved). 18.5 mL Na2CO3 solution (10%) and 1.56 g (10.4 mmol) 4-formylphenylboronic acid are added. After addition of 0.35 g (0.43 mmol) 1,1′-bis(diphenylphosphino)ferrocenedichloropalladium(II) the reaction mixture is purged 3× with argon and heated to 90° C. After 18 h stirring at 90° C. complete dissolution has taken place. The reaction mixture is cooled down and treated with 100 mL water and 150 mL dichloromethane. After vigorous stirring at rt for one hour the organic phase is separated, washed twice with water (100 mL each) and dried (Na2SO4). After removal of the solvent the crude product is purified via chromatography (Isolute, dichloromethane/methanol). 1.82 g (61.5%) of the pure compound and 0.82 g (27.7%) of the product containing traces of the starting material have been obtained.

後処理

  1. dissolutioncompletely dissolved)
  2. customis purged 3× with argon
  3. dissolutioncomplete dissolution
  4. temperatureThe reaction mixture is cooled down
  5. additiontreated with 100 mL water and 150 mL dichloromethane
  6. stirringAfter vigorous stirring at rt for one hour the organic phase
  7. customis separated
  8. washwashed twice with water (100 mL each)
  9. dry with materialdried (Na2SO4)
  10. customAfter removal of the solvent the crude product
  11. customis purified via chromatography (Isolute, dichloromethane/methanol)
  12. addition1.82 g (61.5%) of the pure compound and 0.82 g (27.7%) of the product containing traces of the starting material
  13. customhave been obtained

出典と根拠

ORDレコード
ord-36d880edd1434811953e49dd9f0c6f69
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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