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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 40214생성일: 2026년 10월 24일

(+-)-2-Butanol → N-((6-phenyl-[1,2,4]triazolo[4,3-b]pyridazin-3-yl)methyl)-7H-purin-6-amine

https://huagongshe.com/ko/reaction/40214

반응식

참여 물질

역할이름HCID투입량
반응물(+-)-2-ButanolHCID 6568—
반응물6-ChloropurineHCID 5359277—
반응물(6-Phenyl-[1,2,4]triazolo[4,3-b]pyridazin-3-yl)methanamineHCID 67501979—
생성물N-((6-phenyl-[1,2,4]triazolo[4,3-b]pyridazin-3-yl)methyl)-7H-purin-6-amineHCID 5769117432.8%

반응 조건

온도100 °C

반응 단계

A 15 mL tube was charged with (6-phenyl-[1,2,4]triazolo[4,3-b]pyridazin-3-yl)methanamine (0.100 g, 0.444 mmol), 6-chloropurine (0.103 g, 0.666 mmol), and sec-butanol (3.00 ml, 32.4 mmol), sealed, then heated in a 100° C. oil bath for 5 hours. The reaction mixture was concentrated and the yellow residue was purified by MPLC using a 40 g RediSep column, eluting with a gradient of 3-8% MeOH/DCM over 80 minutes. N-((6-phenyl-[1,2,4]triazolo[4,3-b]pyridazin-3-yl)methyl)-7H-purin-6-amine (0.0500 g, 32.8% yield) was isolated as the hydrochloride salt.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08524900B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-9906acc1e70341139e36a3119039e418
출처 메모uspto-grants-2013_09