Potassium Phosphate, Tribasic → 4-(2-Fluoro-4-trimethylsilanylphenylamino)-1-(toluene-4-sulfonyl)-1H-indazole-5-carboxylic acid methyl ester

HRID 79015ノート

反応式

HRID 79015 の反応式
[CH3:1][O:2][C:3]([C:5]1[C:6](Cl)=[C:7]2[C:11](=[CH:12][CH:13]=1)[N:10]([S:14]([C:17]1[CH:22]=[CH:21][C:20]([CH3:23])=[CH:19][CH:18]=1)(=[O:16])=[O:15])[N:9]=[CH:8]2)=[O:4].COC(=O)/C(=C(\Cl)/C1C(C)=NN(S(C2C=CC(C)=CC=2)(=O)=O)C=1)/C=C.[F:50][C:51]1[CH:56]=[C:55]([Si:57]([CH3:60])([CH3:59])[CH3:58])[CH:54]=[CH:53][C:52]=1[NH2:61].P([O-])([O-])([O-])=O.[K+].[K+].[K+]>C1(C)C=CC=CC=1.C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.[Pd].[Pd]>[CH3:1][O:2][C:3]([C:5]1[C:6]([NH:61][C:52]2[CH:53]=[CH:54][C:55]([Si:57]([CH3:59])([CH3:58])[CH3:60])=[CH:56][C:51]=2[F:50])=[C:7]2[C:11](=[CH:12][CH:13]=1)[N:10]([S:14]([C:17]1[CH:22]=[CH:21][C:20]([CH3:23])=[CH:19][CH:18]=1)(=[O:16])=[O:15])[N:9]=[CH:8]2)=[O:4]

参加物

7

反応物 4

HCID 62657Potassium Phosphate, TribasicHCID 595965992-Fluoro-4-(trimethylsilyl)anilineHCID 670841244-Chloro-1-(toluene-4-sulfonyl)-1H-indazole-5-carboxylic acid methyl esterHCID 872622922-[1-chloro-1-[3-methyl-1-(toluene-4-sulfonyl)-1H-pyrazol-4-yl]-meth-(Z)-ylidene]-but-3-enoic acid methyl ester

生成物 1

HCID 670839874-(2-Fluoro-4-trimethylsilanylphenylamino)-1-(toluene-4-sulfonyl)-1H-indazole-5-carboxylic acid methyl ester収率 50%

試薬・触媒・溶媒 2

HCID 9811564Bis(dibenzylideneacetone)palladium触媒HCID 1140Toluene溶媒

反応条件

温度
105 °C

実験手順

4-Chloro-1-(toluene-4-sulfonyl)-1H-indazole-5-carboxylic acid methyl ester and 2-[1-chloro-1-[3-methyl-1-(toluene-4-sulfonyl)-1H-pyrazol-4-yl]-meth-(Z)-ylidene]-but-3-enoic acid methyl ester (1.1 g, 3.0 mmol), 2-fluoro-4-trimethylsilanylphenylamine (0.61 g, 3.3 mmol), 2-dicyclohexylphosphino-2′-6′-diisopropyl biphenyl (0.28 g, 0.60 mmol), potassium phosphate (0.70 g, 3.3 mmol) and tris(dibenzylideneacetone)dipalladium (0) (87 mg, 0.15 mmol) were suspended in toluene (5 mL) and the resultant mixture degassed. The reaction mixture was heated at 105° C. for 3 hours. The reaction was quenched by the addition of hydrochloric acid (1M, 5 mL) and the resultant mixture extracted with ethyl acetate (3×20 mL). The combined organic extracts were washed with brine (20 mL), dried (MgSO4) and concentrated in vacuo. The resultant residue was subjected to flash chromatography (Si—SPE, gradient 0-100% DCM in cyclohexane) to yield the title compound as a pale brown solid (0.78 g, 50%). 1H NMR showed the product to be a single isomer. LCMS (Method B): RT=5.22 min, [M+H]+=512.

後処理

  1. customthe resultant mixture degassed
  2. customThe reaction was quenched by the addition of hydrochloric acid (1M, 5 mL)
  3. extractionthe resultant mixture extracted with ethyl acetate (3×20 mL)
  4. washThe combined organic extracts were washed with brine (20 mL)
  5. dry with materialdried (MgSO4)
  6. concentrationconcentrated in vacuo

出典と根拠

ORDレコード
ord-304e2d60bf064880b12e7a6abdcfbff8
出典データセット
uspto-grants-2014_09
特許番号
US08841462B2

反応ノート

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