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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1517315생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1517315

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 번호US08232284B2
출처 데이터셋uspto-grants-2012_07
ORD IDord-08749f339c7d43c396e39bb3178fb5c4
출처 메모uspto-grants-2012_07