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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1930581생성일: 2026년 10월 26일

3-(Methylaminomethyl)pyridine → 1-(4-(Methyl(pyridin-3-ylmethyl)amino)-2-(4-(oxazol-5-yl)phenylamino)-7,8-dihydropyrido[4,3-d]pyrimidin-6(5H)-yl)ethanone

https://huagongshe.com/reaction/1930581

반응식

참여 물질

역할이름HCID투입량
반응물3-(Methylaminomethyl)pyridineHCID 88393—
반응물6-Acetyl-2-(4-(oxazol-5-yl)phenylamino)-5,6,7,8-tetrahydropyrido[4,3-d]pyrimidin-4-yl trifluoromethanesulfonateHCID 59333760—
용매Dimethyl SulfoxideHCID 679—
생성물1-(4-(Methyl(pyridin-3-ylmethyl)amino)-2-(4-(oxazol-5-yl)phenylamino)-7,8-dihydropyrido[4,3-d]pyrimidin-6(5H)-yl)ethanoneHCID 4619865353.3%

반응 단계

6-Acetyl-2-(4-(oxazol-5-yl)phenylamino)-5,6,7,8-tetrahydropyrido[4,3-d]pyrimidin-4-yl trifluoromethanesulfonate (35 mg, 0.07 mmol, Example 26a) in DMSO (1 mL) was dispensed in a library plate. N-methyl-1-(pyridin-3-yl)methanamine (8.55 mg, 0.07 mmol) was added and it was left to shake overnight at 80° C. before filtered and purified by preparative HPLC to yield 1-(4-(Methyl(pyridin-3-ylmethyl)amino)-2-(4-(oxazol-5-yl)phenylamino)-7,8-dihydropyrido[4,3-d]pyrimidin-6(5H)-yl)ethanone (17 mg, 52%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08188101B2
출처 데이터셋uspto-grants-2012_05
ORD IDord-424b3be5cee147289094832edea6de91
출처 메모uspto-grants-2012_05