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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 711531생성일: 2026년 10월 24일

N,N-Diisopropylmethylamine → (R)-2-(4-Chloro-2-(2,4-dimethoxybenzyl)-7-fluoro-3-oxo-2,3-dihydro-1H-pyrrolo[3,4-c]pyridin-6-ylamino)-4-methylpentanamide

https://huagongshe.com/ko/reaction/711531

반응식

참여 물질

역할이름HCID투입량
반응물N,N-DiisopropylmethylamineHCID 547370—
반응물(R)-2-Amino-4-methylpentanamideHCID 7271815—
반응물4,6-dichloro-2-[(2,4-dimethoxyphenyl)methyl]-7-fluoro-1H,2H,3H-pyrrolo[3,4-c]pyridin-3-oneHCID 58317575—
용매AcetonitrileHCID 6342—
용매MeOH DCM DMFHCID 86602994—
생성물(R)-2-(4-Chloro-2-(2,4-dimethoxybenzyl)-7-fluoro-3-oxo-2,3-dihydro-1H-pyrrolo[3,4-c]pyridin-6-ylamino)-4-methylpentanamideHCID 5831756033.1%

반응 조건

온도85 °C

반응 단계

A mixture of 4,6-dichloro-2-(2,4-dimethoxybenzyl)-7-fluoro-1H-pyrrolo[3,4-c]pyridin-3(2H)-one (200 mg, 0.539 mmol), (R)-2-amino-4-methylpentanamide (140 mg, 1.078 mmol), and N-isopropyl-N-methylpropan-2-amine (310 mg, 2.69 mmol) in acetonitrile (2 mL) was stirred at 85° C. for 3 d. The resulting crude material was reconstituted in MeOH/DCM/DMF (10.0 mL) and purified via preparative HPLC. The fractions were collected and stripped to dryness via rotary evaporation to yield the title compound (83 mg, 33%). [M+H] calc'd for C22H26ClFN4O4, 465. found, 465.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09181255B2
출처 데이터셋uspto-grants-2015_11
ORD IDord-0f611d64ff7f4ba19e623cf1293411c9
출처 메모uspto-grants-2015_11