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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 516072생성일: 2026년 10월 26일

(R)-2-(2-(2,4-dimethoxybenzyl)-7-fluoro-4-(1-methyl-1H-pyrazol-4-yl)-3-oxo-2,3-dihydro-1H-pyrrolo[3,4-c]pyridin-6-ylamino)-4-methylpentanamide → (R)-2-(7-Fluoro-4-(1-methyl-1H-pyrazol-4-yl)-3-oxo-2,3-dihydro-1H-pyrrolo[3,4-c]pyridin-6-ylamino)-4-methylpentanamide

https://huagongshe.com/reaction/516072

반응식

참여 물질

역할이름HCID투입량
반응물(R)-2-(2-(2,4-dimethoxybenzyl)-7-fluoro-4-(1-methyl-1H-pyrazol-4-yl)-3-oxo-2,3-dihydro-1H-pyrrolo[3,4-c]pyridin-6-ylamino)-4-methylpentanamideHCID 58317690—
용매Trifluoroacetic acidHCID 6422—
생성물(R)-2-(7-Fluoro-4-(1-methyl-1H-pyrazol-4-yl)-3-oxo-2,3-dihydro-1H-pyrrolo[3,4-c]pyridin-6-ylamino)-4-methylpentanamideHCID 5325052046%

반응 단계

A solution of (R)-2-(2-(2,4-dimethoxybenzyl)-7-fluoro-4-(1-methyl-1H-pyrazol-4-yl)-3-oxo-2,3-dihydro-1H-pyrrolo[3,4-c]pyridin-6-ylamino)-4-methylpentanamide (39.8 mg, 0.078 mmol) in TFA (5 mL) was heated at 60° C. for 2 h. After removal of solvent, the residue was diluted in MeOH (2 mL) and was purified by preparative HPLC. The fractions were collected and the solvent stripped to dryness via rotary evaporation to yield the title compound (12.8 mg, 46%). 1H NMR (500 MHz, DMSO-d6) δ ppm 0.82-1.00 (m, 6 H), 1.45-1.60 (m, 1 H), 1.67-1.83 (m, 2 H), 3.87 (s, 3 H), 4.36 (s, 2 H), 4.50-4.64 (m, 1 H), 6.88-7.02 (m, 2 H), 7.44 (s, 1 H), 8.28 (s, 2 H), 8.83 (s, 1 H). [M+H] calc'd for C17H21FN6O2, 361; found, 361.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09108970B2
출처 데이터셋uspto-grants-2015_08
ORD IDord-e97622d1063e4aaba99ddea5994c0b02
출처 메모uspto-grants-2015_08