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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 383952생성일: 2026년 10월 26일

1-Azabicyclo(2.2.2)octane-4-methanol → 1-Azabicyclo[2.2.2]oct-4-ylmethyl(5-phenyl-1,3-thiazol-4-yl)carbamate hydrochloride

https://huagongshe.com/reaction/383952

반응식

참여 물질

역할이름HCID투입량
반응물1-Azabicyclo(2.2.2)octane-4-methanolHCID 141311—
반응물P,P-Diphenylphosphinic azideHCID 199401—
반응물Sodium BicarbonateHCID 516892—
반응물5-phenyl-1,3-thiazole-4-carboxylic AcidHCID 944813—
반응물Hydrogen chloride-ethyl acetateHCID 21866389—
용매EthanolHCID 702—
용매TolueneHCID 1140—
용매DimethylformamideHCID 6228—
생성물1-Azabicyclo[2.2.2]oct-4-ylmethyl(5-phenyl-1,3-thiazol-4-yl)carbamate hydrochlorideHCID 68593591—

반응 단계

To a solution of 5-phenyl-1,3-thiazole-4-carboxylic acid (250 mg) in toluene (6 mL) were added dropwise TEA (221 μL) and DPPA (315 μL) at room temperature, followed by stirring at the same temperature for 40 minutes. Next, after stirring at 90° C. for 40 minutes, a solution of 1-azabicyclo[2.2.2]oct-4-yl methanol (241 mg) in DMF (2 mL)/toluene (2 mL) was added thereto, followed by heating under reflux for 2 hours. To the reaction liquid was added a saturated aqueous NaHCO3 solution, followed by extraction with EtOAc. The organic layer was washed with water and brine in this order, dried over MgSO4, and then filtered, and the filtrate was concentrated under reduced pressure. The residue was purified by medium-pressure preparative liquid chromatography (YAMAZEN YFLC WPrep2XY, eluent; CHCl3:MeOH:28% aqueous ammonia=80:10:1) to obtain a yellow oily substance. To this solution in EtOH (2 mL) was added 4 M HCl/EtOAc (1 mL) at room temperature, followed by stirring, and the solvent was concentrated under reduced pressure. The residue obtained was recrystallized from EtOH/ether to obtain 1-azabicyclo[2.2.2]oct-4-ylmethyl(5-phenyl-1,3-thiazol-4-yl)carbamate hydrochloride (145 mg) as a yellow solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08367696B2
출처 데이터셋uspto-grants-2013_02
ORD IDord-a2c76768b18146f9aa68e7fececbfdfd
출처 메모uspto-grants-2013_02