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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 256905생성일: 2026년 10월 26일

1-Bromohexane → 5-(3-Hexylthio-1,2,5-thiadiazol-4-yl)-1-azabicyclo[3.2.1]octane oxalate

https://huagongshe.com/reaction/256905

반응식

참여 물질

역할이름HCID투입량
반응물1-BromohexaneHCID 8101—
반응물Potassium CarbonateHCID 11430—
반응물Sodium hydrosulfide hydrateHCID 16211346—
반응물5-(3-Chloro-1,2,5-thiadiazol-4-yl)-1-azabicyclo[3.2.1]octane oxalateHCID 21708609—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물5-(3-Hexylthio-1,2,5-thiadiazol-4-yl)-1-azabicyclo[3.2.1]octane oxalateHCID 2170863949.8%

반응 단계

Sodium hydrosulfide monohydrate (326 mg, 4.4 mmol) was added to a solution of 5-(3-chloro-1,2,5-thiadiazol-4-yl)-1-azabicyclo[3.2.1]octane oxalate (350 mg, 1.1 mmol) in DMF (20 ml) at room temperature and the reaction mixture was stirred for 30 min. Potassium carbonate (1.24 g, 9 mmol) and 1-bromohexan (561 μl, 4 mmol) were added and the reaction mixture was stirred for 3 h. Water (50 ml) was added to the reaction mixture and the aqueous phase extracted with ether (3×200 ml). The combined ether phases were dried and evaporated to give the crude free base of the title compound (220 mg). The residue was crystallized as the oxalate salt from acetone to give the title compound. Yield 200 mg (Compound 68), m.p. 67°-69° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05260314
출처 데이터셋uspto-grants-1993_11
ORD IDord-d53536103116448e8dcae9823fbf6f66
출처 메모uspto-grants-1993_11