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HRID 1516831作成日:2026年10月26日

Trifluoroacetic acid → 4-(4-(4-cyclopropyl-2,6-dimethylphenoxy)-7H-pyrrolo[2,3-d]pyrimidin-2-ylamino)benzonitrile

https://huagongshe.com/reaction/1516831

反応式

関与物質

役割名称HCID仕込み量
反応物Trifluoroacetic acidHCID 6422—
反応物4-AminobenzonitrileHCID 13396—
反応物2-chloro-4-(4-cyclopropyl-2,6-dimethylphenoxy)-7H-pyrrolo[2,3-d]pyrimidineHCID 57693576—
溶媒2,2,2-TrifluoroethanolHCID 6409—
溶媒Ethyl AcetateHCID 8857—
生成物4-(4-(4-cyclopropyl-2,6-dimethylphenoxy)-7H-pyrrolo[2,3-d]pyrimidin-2-ylamino)benzonitrileHCID 5769359416%

反応条件

温度90 °C

反応手順

To a suspension of 2-chloro-4-(4-cyclopropyl-2,6-dimethylphenoxy)-7H-pyrrolo[2,3-d]pyrimidine (75 mg, 0.24 mmol) and 4-aminobenzonitrile (113 mg, 0.96 mmol) in 2,2,2-trifluoroethanol (4 mL) in a sealed tube was added trifluoroacetic acid (0.15 mL, 1.92 mmol). The resulting solution was heated at 90° C. for 3 days. The reaction was diluted with EtOAc (50 mL), washed with NaHCO3 (20 mL) and brine (20 mL), dried with Na2SO4, and concentrated to dryness. Silica gel chromatography (CH2Cl2:Acetone 90:10) yielded 15 mg (16%) of 4-(4-(4-cyclopropyl-2,6-dimethylphenoxy)-7H-pyrrolo[2,3-d]pyrimidin-2-ylamino)benzonitrile as a tan solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08227601B2
出典データセットuspto-grants-2012_07
ORD IDord-fe63115a37c4489cb07bc8368d16dd2d
出典メモuspto-grants-2012_07