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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 40149생성일: 2026년 10월 24일

2-Pyrrolidone → 1-Benzyl-N-(3,4-difluorobenzyl)-6-(3,4-dihydro-2H-pyrrol-5-ylamino)-5-fluoro-2-isopropyl-1H-indole-3-carboxamide

https://huagongshe.com/ko/reaction/40149

반응식

참여 물질

역할이름HCID투입량
반응물2-PyrrolidoneHCID 12025—
반응물Phosphorus oxychlorideHCID 24813—
반응물6-amino-1-benzyl-N-(3,4-difluorobenzyl)-5-fluoro-2-isopropyl-1H-indole-3-carboxamideHCID 59762400—
용매TolueneHCID 1140—
용매Ethyl AcetateHCID 8857—
생성물1-Benzyl-N-(3,4-difluorobenzyl)-6-(3,4-dihydro-2H-pyrrol-5-ylamino)-5-fluoro-2-isopropyl-1H-indole-3-carboxamideHCID 59762436—

반응 조건

온도110 °C

반응 단계

A mixture of 2-pyrrolidinone (47 mg, 0.55 mmol) and POCl3 (0.10 ml, 1.1 mmol) was stirred at 0° C. to room temperature for 2h. To the above mixture was then added a solution of 6-amino-1-benzyl-N-(3,4-difluorobenzyl)-5-fluoro-2-isopropyl-1H-indole-3-carboxamide (Compound 172, 50 mg, 0.11 mmol) in toluene (3 ml). The reaction was heated to 110° C. for 16 h and was cooled to room temperature, diluted with EtOAc, washed with brine, dried over Na2SO4, and concentrated in vacuo. The residue was purified by reverse phase chromatography on C18 bonded silica gel (MeOH) to yield the title compound as a white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08524917B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-87efb787dd884b16baaff4567165b540
출처 메모uspto-grants-2013_09