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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1607064생성일: 2026년 10월 25일

Ammonia → Ether 3-[4-(3-amino-5-bromopyrid-2-yl)butylamino]-4-amino-1,2,5-thiadiazole-1-oxide

https://huagongshe.com/reaction/1607064

반응식

참여 물질

역할이름HCID투입량
반응물AmmoniaHCID 222—
반응물3,4-Dimethoxy-1,2,5-thiadiazole 1-oxideHCID 12913947—
반응물3-Amino-5-bromo-(4-aminobutyl)pyridineHCID 14537459—
반응물3-[4-(3-Amino-5-bromopyrid-2-yl)butylamino]-4-methoxy-1,2,5-thiadiazole-1-oxideHCID 15962360—
반응물4-(3-Amino-5-bromopyrid-2-yl)-4-methoxy-1,2,5-thiadiazole-1-oxideHCID 86743353—
용매MethanolHCID 887—
용매ChloroformHCID 6212—
생성물Ether 3-[4-(3-amino-5-bromopyrid-2-yl)butylamino]-4-amino-1,2,5-thiadiazole-1-oxideHCID 867402109.7%

반응 단계

A solution of 3,4-dimethoxy-1,2,5-thiadiazole-1-oxide (0.995 g) in methanol (25 ml) was reacted with a solution of 3-amino-5-bromo-(4-aminobutyl)pyridine (1.5 g) in methanol (25 ml) at room temperature for 3 hours. The solvent was removed in vacuo and the residue was chromatographed on silica in ethanol to give an oil which was triturated with ether and recrystallised from ethanol/ether to give 3-[4-(3-amino-5-bromopyrid-2-yl) butylamino]-4-methoxy-1,2,5-thiadiazole-1-oxide (1.7 g) m.p. 118°-120° C. (g) Reaction of 3-[4-(3-amino-5-bromopyrid-2-yl)-4-methoxy-1,2,5-thiadiazole-1-oxide (0.56 g) with methanolic ammonia solution (50 ml) at room temperature overnight gave after chromatography on silica in chloroform and trituration with ether 3-[4-(3-amino-5-bromopyrid-2-yl)butylamino]-4-amino-1,2,5-thiadiazole-1-oxide (0.19 g) m.p. 105°-109° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04863936
출처 데이터셋uspto-grants-1989_09
ORD IDord-357272ff030e41c1ab1609e5f6bd04f6
출처 메모uspto-grants-1989_09