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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 274271생성일: 2026년 10월 24일

5-Hydroxy-4,4-dimethyl-1-pentanesulfonamide → 1-Pentanesulfonamide, 4,4-dimethyl-5-((7-methyl(1,2,4)triazolo(1,5-b)pyridazin-6-yl)oxy)-

https://huagongshe.com/ko/reaction/274271

반응식

참여 물질

역할이름HCID투입량
반응물5-Hydroxy-4,4-dimethyl-1-pentanesulfonamideHCID 10726520—
반응물6-Chloro-7-methyl-[1,2,4]triazolo[1,5-b]pyridazineHCID 11805158—
생성물1-Pentanesulfonamide, 4,4-dimethyl-5-((7-methyl(1,2,4)triazolo(1,5-b)pyridazin-6-yl)oxy)-HCID 3073788—

반응 단계

Using 5-hydroxy-4,4-dimethyl-1-pentanesulfonamide and 6-chloro-7-methyl[1,2,4]triazolo[1,5-b]pyridazine, the same reaction was conducted as in Example 5 to produce the title compound. m.p. 171°-172° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05389633
출처 데이터셋uspto-grants-1995_02
ORD IDord-55d85fa45f36489eabca2860c9c974a7
출처 메모uspto-grants-1995_02