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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 15452생성일: 2026년 10월 23일

1-Hydroxybenzotriazole → rac-N-(1-Azabicyclo[2.2.2]oct-3-yl)-5-nitro-1-benzothiophene-2-carboxamide hydrochloride

https://huagongshe.com/ko/reaction/15452

반응식

참여 물질

역할이름HCID투입량
반응물1-HydroxybenzotriazoleHCID 75771—
반응물5-Nitro-2-thenoic acidHCID 80591—
반응물DiisopropylethylamineHCID 81531—
반응물Quinuclidine, 3-amino-, dihydrochlorideHCID 197853—
반응물O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
용매DimethylformamideHCID 6228—
생성물rac-N-(1-Azabicyclo[2.2.2]oct-3-yl)-5-nitro-1-benzothiophene-2-carboxamide hydrochlorideHCID 1019383348.6%

반응 단계

At RT, initially 244 mg (0.76 mmol) of TBTU and 104 mg (0.78 mmol) of HOBt followed by 153 mg (0.77 mmol) of 3-aminoquinuclidine dihydrochloride are added to a solution of 180 mg (0.81 mmol) of 5-nitrothiophene-2-carboxylic acid and diiso-propylethylamine (0.8 ml) in 4 ml of DMF. The mixture is stirred at RT for 4 h. For work-up, the mixture is concentrated and the residue is taken up in a mixture of chloroform and excess aqueous sodium hydroxide solution. The phases are separated and the aqueous phase is repeatedly re-extracted with chloroform. The combined organic phases are dried over sodium sulfate and concentrated, and the crude product is chromatographed on silica gel (mobile phase: chloroform/methanol/conc. ammonia 100:5:0.5→100:20:2). The resulting product is taken up in THF, excess HCl in diethyl ether is added, then the mixture is concentrated and the product is dried under high vacuum. 136 mg (47% of theory) of the hydrochloride are obtained.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07732477B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-f37e172f2ee944e69c1eea23992947aa
출처 메모uspto-grants-2010_06