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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 384723생성일: 2026년 10월 25일

Triethylamine → tert-Butyl 4-((6-(5-cyano-6-methoxypyrazin-2-ylamino)pyrimidin-4-ylamino)methyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/384723

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물1-Boc-4-(aminomethyl)piperidineHCID 736817—
반응물5-(6-Chloropyrimidin-4-ylamino)-3-methoxypyrazine-2-carbonitrileHCID 59613517—
용매AcetonitrileHCID 6342—
생성물tert-Butyl 4-((6-(5-cyano-6-methoxypyrazin-2-ylamino)pyrimidin-4-ylamino)methyl)piperidine-1-carboxylateHCID 5961347340.1%

반응 단계

A solution of 5-(6-chloropyrimidin-4-ylamino)-3-methoxypyrazine-2-carbonitrile (4.5 mg, 0.017 mmol), tert-butyl 4-(aminomethyl)piperidine-1-carboxylate (4 mg, 0.034 mmol) and triethylamine (12 uL, 0.085 mmol) in acetonitrile (1.5 mL) was heated at 145° C. for 90 min using microwave irradiation. The solvent was removed in vacuo and the crude mixture was purified by preparative thin layer chromatography, eluting with dichloromethane/MeOH (10/1), to give the title compound as a yellow oil (3 mg, 40%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08367658B2
출처 데이터셋uspto-grants-2013_02
ORD IDord-1d2eebfb2a714ea885b557fbc721b2cf
출처 메모uspto-grants-2013_02