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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 724308생성일: 2026년 10월 26일

Triethylamine → HCID 178503265, 화합물

https://huagongshe.com/reaction/724308

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물1-HydroxybenzotriazoleHCID 75771—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
반응물2-(4-Methylsulfanyl-phenoxy)-nicotinic acidHCID 21877137—
반응물HCID 178479277HCID 178479277—
용매DimethylformamideHCID 6228—
생성물AmmoniaHCID 222—
생성물HCID 178503265HCID 178503265181.1%

반응 단계

2-(4-Methylsulfanyl-phenoxy)-nicotinic acid (500 mg, 1.91 mmol) was dissolved in dimethylformamide (10 ml) and triethylamine (800 μl, 5.74 mmol) was added followed by cis-4-aminocyclohexanol hydrochloride (290 mg, 1.91 mmol), 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (404 mg, 2.10 mmol) and 1-hydroxybenzotriazole (284 mg, 2.10 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 sat. sodium bicarbonate solution (25 ml) and ethyl acetate (20 ml) and the aqueous phase was extracted with ethyl acetate (2×20 ml). The combined organic extracts were washed with water (10 ml), brine (10 ml), dried over MgSO4 and the solvent was removed under reduced pressure. The residue was purified by flash column chromatography on silica gel eluting with a solvent gradient of dichloromethane:methanol:concentrated aqueous ammonia (97.5:2.5:0.25 changing to 97:3:0.3, by volume) to give N-(cis-4-hydroxy-cyclohexyl)-2-(4-methylsulfanyl-phenoxy)-nicotinamide (620 mg) as a white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07141586B2
출처 데이터셋uspto-grants-2006_11
ORD IDord-d69468b24ee649bd9f4183ae2642de3b
출처 메모uspto-grants-2006_11