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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 516113생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/516113

반응식

참여 물질

역할이름HCID투입량
반응물(R)-2-(2-(2,4-Dimethoxybenzyl)-7-fluoro-4-(furan-2-yl)-3-oxo-2,3-dihydro-1H-pyrrolo[3,4-c]pyridin-6-ylamino)-4-methylpentanamideHCID 58317552—
용매Trifluoroacetic acidHCID 6422—
생성물(R)-2-(7-Fluoro-4-(furan-2-yl)-3-oxo-2,3-dihydro-1H-pyrrolo[3,4-c]pyridin-6-ylamino)-4-methylpentanamideHCID 58317542—

반응 단계

A solution of (R)-2-(2-(2,4-dimethoxybenzyl)-7-fluoro-4-(furan-2-yl)-3-oxo-2,3-dihydro-1H-pyrrolo[3,4-c]pyridin-6-ylamino)-4-methylpentanamide (93.1 mg, 0.188 mmol) in TFA (5 mL) was heated to 65° C. for 3 h. The solvent was removed and the resulting residue was diluted in MeOH/DCM (10 mL) and was purified via preparative HPLC eluting with water (0.05% TFA) and ACN (30%, 0.035% TFA). The collected fractions were stripped to dryness via rotary evaporation to afford the title compound. 1H NMR (400 MHz, DMSO-d6) δ ppm 0.79-0.97 (m, 6 H), 1.52-1.87 (m, 3 H), 4.38 (s, 2 H), 4.66-4.85 (m, 1 H), 6.61 (dd, J=3.54, 1.77 Hz, 1 H), 6.92-7.07 (m, 2 H), 7.36 (br s, 1 H), 7.79 (dd, J=1.64, 0.63 Hz, 1 H), 8.04 (dd, J=3.54, 0.51 Hz, 1 H), 8.32 (s, 1 H). [M+H] calc'd for C17H19FN4O3, 347; found, 347.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09108970B2
출처 데이터셋uspto-grants-2015_08
ORD IDord-81576e95df1046778f44058f68138758
출처 메모uspto-grants-2015_08