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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 225502생성일: 2026년 10월 26일

Triethylamine → 4-[(3-Oxo-1-piperazinyl)methyl]-N-[4-methyl-3-[[4-(3-pyridinyl)-2-pyrimidinyl]amino]phenyl]benzamide

https://huagongshe.com/reaction/225502

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Sodium BicarbonateHCID 516892—
반응물Propylphosphoric anhydrideHCID 16167369—
반응물4-((3-Oxopiperazin-1-yl)methyl)benzoic acidHCID 16777099—
반응물N-(3-amino-4-methylphenyl)-4-(pyridin-3-yl)-2-pyrimidine-amineHCID 24820369—
용매DimethylformamideHCID 6228—
생성물4-[(3-Oxo-1-piperazinyl)methyl]-N-[4-methyl-3-[[4-(3-pyridinyl)-2-pyrimidinyl]amino]phenyl]benzamideHCID 10217696—

반응 단계

A solution of propylphosphonic anhydride in N,N-dimethylformamide (Fluka, Buchs, Switzerland; 1.3 mL of 50%, 2.25 mmol) is added dropwise to a stirred mixture of 4-methyl-N-[4-(3-pyridinyl)-2-pyrimidinyl]-1,3-benzenediamine (416 mg, 1.5 mmol), 4-[(3-oxo-1-piperazinyl)methyl]benzoic acid (351 mg, 1.5 mmol) and triethylamine (1.7 mL, 12 mmol) in dry N,N-dimethylformamide (4 mL). The mixture is stirred for 17 hours at room temperature and then treated with saturated aqueous sodium hydrogen carbonate solution (100 mL). The resulting precipitate is filtered, washed with water, dried and recrystallised from methanol to give the title compound as a cream crystalline solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07557105B2
출처 데이터셋uspto-grants-2009_07
ORD IDord-c3e61f6688dc4d85bd0d7f3e4111673b
출처 메모uspto-grants-2009_07