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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 657774생성일: 2026년 10월 25일

Acetonitrile → 5-bromo-2-(4-((6-(trifluoromethyl)pyridin-3-yl)methylamino)-7,8-dihydropyrido[4,3-d]pyrimidin-6(5H)-yl)benzonitrile

https://huagongshe.com/reaction/657774

반응식

참여 물질

역할이름HCID투입량
반응물AcetonitrileHCID 6342—
반응물DiisopropylethylamineHCID 81531—
반응물5-Bromo-2-fluorobenzonitrileHCID 2724900—
반응물N-((6-(trifluoromethyl)pyridin-3-yl)methyl)-5,6,7,8-tetrahydropyrido[4,3-d]pyrimidin-4-amineHCID 59840682—
용매Ethyl AcetateHCID 8857—
생성물5-bromo-2-(4-((6-(trifluoromethyl)pyridin-3-yl)methylamino)-7,8-dihydropyrido[4,3-d]pyrimidin-6(5H)-yl)benzonitrileHCID 2506187157.5%

반응 단계

A mixture of N-((6-(trifluoromethyl)pyridin-3-yl)methyl)-5,6,7,8-tetrahydropyrido[4,3-d]pyrimidin-4-amine (1.0 g, 3.2 mmol), 5-bromo-2-fluorobenzonitrile (0.97 g, 4.8 mmol), N,N-diisopropylethylamine (1.7 mL, 9.7 mmol), and acetonitrile (10 mL) was subjected to microwave irradiation at 180° C. for 2 h. More 5-bromo-2-fluorobenzonitrile (1.0 g) was added and the mixture was subjected to microwave irradiation at 180° C. for another 2 h. Then additional 5-bromo-2-fluorobenzonitrile (1.0 g) was added and the reaction mixture was subjected to microwave irradiation at 180° C. for an additional 2 h. After cooling, the mixture was diluted with EtOAc (100 mL) and washed with aq. Na2CO3 solution and brine, dried (Na2SO4) and concentrated. The residue was purified by silica gel column (100% EtOAc) to yield a light yellow solid (0.90 g, 57%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08076345B2
출처 데이터셋uspto-grants-2011_12
ORD IDord-f00fdbe4c14c4cec8edc5b231ec9c077
출처 메모uspto-grants-2011_12