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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1516857생성일: 2026년 10월 26일

Trifluoroacetic acid → 4-(4-(4-Acetyl-2,6-dimethylphenoxy)-5-benzyl-5H-pyrrolo[3,2-d]pyrimidin-2-ylamino)benzonitrile

https://huagongshe.com/reaction/1516857

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참여 물질

역할이름HCID투입량
반응물Trifluoroacetic acidHCID 6422—
반응물4-AminobenzonitrileHCID 13396—
반응물1-(4-(5-benzyl-2-chloro-5H-pyrrolo[3,2-d]pyrimidin-4-yloxy)-3,5-dimethylphenyl)ethanoneHCID 57693554—
용매WaterHCID 962—
생성물4-(4-(4-Acetyl-2,6-dimethylphenoxy)-5-benzyl-5H-pyrrolo[3,2-d]pyrimidin-2-ylamino)benzonitrileHCID 5769364251.7%

반응 조건

온도90 °C

반응 단계

In a sealed tube was added 1-(4-(5-benzyl-2-chloro-5H-pyrrolo[3,2-d]pyrimidin-4-yloxy)-3,5-dimethylphenyl)ethanone (111 mg, 0.27 mmol), 4-aminobenzonitrile (129 mg, 1.1 mmol), TFE (1.7 mL) and TFA (0.2 mL, 2.16 mmol). The reaction mixture was stirred at 90° C. for 16 h. Upon completion of the reaction, the resulting mixture was cooled, diluted with water, and washed with EtOAc. The combined organic layers were washed with NaHCO3 and brine; dried over Na2SO4; filtered; and concentrated in vacuo. The crude product was purified by silica gel column chromatography, eluting with hexanes:ethyl acetate (9:1-100% EtOAc), to give the product as an off-white solid (68 mg, 51%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08227601B2
출처 데이터셋uspto-grants-2012_07
ORD IDord-04e84c98afee4a6786596d6f72b6a209
출처 메모uspto-grants-2012_07