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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 724292생성일: 2026년 10월 27일

Triethylamine → N-cyclohexyl-2-[3-(methylsulfanyl)phenoxy]nicotinamide

https://huagongshe.com/reaction/724292

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물1-HydroxybenzotriazoleHCID 75771—
반응물Cyclohexylamine hydrochlorideHCID 2723770—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
반응물2-[3-(Methylsulfanyl)phenoxy]nicotinic acidHCID 21877174—
용매DimethylformamideHCID 6228—
생성물N-cyclohexyl-2-[3-(methylsulfanyl)phenoxy]nicotinamideHCID 2187714650.8%

반응 단계

2-[3-(Methylsulfanyl)phenoxy]nicotinic acid (200 mg, 0.77 mmol) was dissolved in dimethylformamide (5 ml) and triethylamine (427 ul, 3.07 mmol) was added followed by cyclohexylamine hydrochloride (88 ug, 0.77 mmol), 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (294 mg, 1.53 mmol) and 1-hydroxybenzotriazole (114 mg, 0.84 mmol). The reaction was stirred under nitrogen at room temperature for 18 h and the solvent was removed under reduced pressure. The residue was partitioned between water (50 ml) and diethyl diethyl ether (50 ml). The organic phase was washed with brine, dried over MgSO4 and the solvent was removed under reduced pressure. The residue was purified by flash column chromatography using ethyl acetate:cyclohexane (20:80 to 35:65) as eluant to give a white solid which was recrystallised from diethyl diethyl ether/pentane to give N-cyclohexyl-2-[3-(methylsulfanyl)phenoxy]nicotinamide (134 mg) as a white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07141586B2
출처 데이터셋uspto-grants-2006_11
ORD IDord-e25ada4368444a8c94c1a94fde460c4e
출처 메모uspto-grants-2006_11