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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 81680생성일: 2026년 10월 26일

Triethylamine → 5,6-dichloro-N-[3-(dimethylamino)propyl]-N-methylnicotinamide

https://huagongshe.com/reaction/81680

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참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Thionyl ChlorideHCID 24386—
반응물1,3-Propanediamine, N1,N1,N3-trimethyl-HCID 78302—
반응물5,6-Dichloronicotinic acidHCID 247987—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물5,6-dichloro-N-[3-(dimethylamino)propyl]-N-methylnicotinamideHCID 636953660.1%

반응 조건

온도90 °C

반응 단계

Thionyl chloride (15 ml) was added to 5,6-dichloronicotinic acid (2.0 g, 10.4 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 (4.36 ml, 31.3 mmol) and N,N,N′-trimethylpropane-1,3-diamine (2.39 ml, 15.6 mmol) were added to a tetrahydrofuran solution (30 ml) of the obtained residue, and stirred at room temperature for 3 minutes. Saturated saline water was added to the reaction solution, and extracted with chloroform. 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-[3-(dimethylamino)propyl]-N-methylnicotinamide (3.21 mg) as an orange oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08846700B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-61ca127fc5f349d4ac5d2a6b922adcf8
출처 메모uspto-grants-2014_09