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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 81676생성일: 2026년 10월 24일

Triethylamine → 5,6-dichloro-N-methyl-N-(2-pyrrolidin-1-ylethyl)nicotinamide

https://huagongshe.com/ko/reaction/81676

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Thionyl ChlorideHCID 24386—
반응물5,6-Dichloronicotinic acidHCID 247987—
반응물Methyl(2-(pyrrolidin-1-yl)ethyl)amineHCID 295976—
용매WaterHCID 962—
용매ChloroformHCID 6212—
용매TetrahydrofuranHCID 8028—
생성물5,6-dichloro-N-methyl-N-(2-pyrrolidin-1-ylethyl)nicotinamideHCID 55161862102.2%

반응 조건

온도90 °C

반응 단계

Thionyl chloride (6 ml) was added to 5,6-dichloronicotinic acid (600 mg, 3.13 mmol), and stirred under a nitrogen atmosphere at 90° C. for 30 minutes. The reaction solution was concentrated under reduced pressure, and with cooling with ice, triethylamine (1.31 ml, 9.38 mmol) and N-methyl-2-pyrrolidin-1-ylethanamine (481 mg, 3.75 mmol) were added to a tetrahydrofuran solution (4 ml) of the obtained residue, and stirred at room temperature for 3 minutes. Saturated saline water and chloroform were added to the reaction solution, the organic layer was dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The obtained residue was purified by amine-type silica gel column chromatography (Biotage NH, hexane:ethyl acetate=4:1 to 1:1) to obtain 5,6-dichloro-N-methyl-N-(2-pyrrolidin-1-ylethyl)nicotinamide 967 mg) as an orange oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08846700B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-b7936fa6667c445584f1ffe69e8e3eb8
출처 메모uspto-grants-2014_09