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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 353983생성일: 2026년 10월 24일

Triethylamine → N-(4-Cyano-1-methyl-piperidin-4-yl)-3-cyclohexyl-2-(3-diethylamino-carbonyl-thioureido)-propionamide

https://huagongshe.com/reaction/353983

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물N,N-Diethyl carbamoyl thiocyanateHCID 22063149—
반응물2-amino-N-(-4-cyano-1-propyl-piperidin-4-yl)-3-cyclohexylpropionamide bis hydrochloride saltHCID 86585200—
용매AcetonitrileHCID 6342—
생성물N-(4-Cyano-1-methyl-piperidin-4-yl)-3-cyclohexyl-2-(3-diethylamino-carbonyl-thioureido)-propionamideHCID 8659645449%

반응 단계

A solution of 2-amino -N-(-4-cyano-1-propyl-piperidin-4-yl)-3-cyclohexylpropionamide bis hydrochloride salt (560 mg, 1.53 mmol) and triethylamine (500 μL, 3.59 mmol) in acetonitrile (4 mL) was treated with a solution of N,N-diethyl carbamoyl thiocyanate in acetonitrile (3.0 mL, 2.7 mmol). The reaction mixture was stirred overnight at room temperature and concentrated on a rotary evaporator. The resulting residue was chromatographed (ethyl acetate:hexanes 1:1 then ethyl acetate and finally methanol:methylene chloride 1:9 as the eluant) to provide the desired product as a light yellow solid (340 mg, 49%). MS, m/z 451.3=M+1.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06756372B2
출처 데이터셋uspto-grants-2004_06
ORD IDord-c1aedbbd022e47b681476c8922264332
출처 메모uspto-grants-2004_06