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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1045511생성일: 2026년 10월 27일

3-Fluorobenzoic Acid → 3-fluoro-N-(6-{[3-(4-methoxybenzyl)-2-oxo-1,2,3,4-tetrahydropyrido[2,3-d]pyrimidin-5-yl]oxy}-1-methyl-1H-indazol-3-yl)benzamide

https://huagongshe.com/reaction/1045511

반응식

참여 물질

역할이름HCID투입량
반응물3-Fluorobenzoic AcidHCID 9968—
반응물DiisopropylethylamineHCID 81531—
반응물5-[(3-amino-1-methyl-1H-indazol-6-yl)oxy]-3-(4-methoxybenzyl)-3,4-dihydropyrido[2,3-d]pyrimidin-2(1H)-oneHCID 70497185—
용매DimethylformamideHCID 6228—
생성물3-fluoro-N-(6-{[3-(4-methoxybenzyl)-2-oxo-1,2,3,4-tetrahydropyrido[2,3-d]pyrimidin-5-yl]oxy}-1-methyl-1H-indazol-3-yl)benzamideHCID 6692644526%

반응 조건

온도100 °C

반응 단계

A solution of 5-[(3-amino-1-methyl-1H-indazol-6-yl)oxy]-3-(4-methoxybenzyl)-3,4-dihydropyrido[2,3-d]pyrimidin-2(1H)-one (100.00 mg; 0.23 mmol; 1.00 eq.),3-fluorobenzoic acid (35.80 mg; 0.26 mmol; 1.10 eq.), pybop (157.16 mg; 0.30 mmol; 1.30 eq.), DMF (4.00 ml), and N,N-diisopropylethylamine (115.48 μl; 0.70 mmol; 3.00 eq.) was stirred at room temperature for 22 hr. Additional pybop was added and the reaction was heated to 100 degrees C. but the reaction did not go to completion. The reaction was concentrated, redissolved in DMSO, and purified via prep HPLC to afford 17 mg (26%) of 3-fluoro-N-(6-{[3-(4-methoxybenzyl)-2-oxo-1,2,3,4-tetrahydropyrido[2,3-d]pyrimidin-5-yl]oxy}-1-methyl-1H-indazol-3-yl)benzamide as a yellow solid. LC-MS (M+H=553, obsd.=553).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08569295B2
출처 데이터셋uspto-grants-2013_10
ORD IDord-12c80b5c4645413b881a02e34ef205a6
출처 메모uspto-grants-2013_10