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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1818189생성일: 2026년 10월 27일

Triethylamine → N-{2-[4-amino-2-butyl-7-(pyridin-3-yl)-1H-imidazo[4,5-c]quinolin-1-yl]ethyl}-2-methylpropanamide

https://huagongshe.com/reaction/1818189

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Isobutyryl chlorideHCID 62325—
반응물1-(2-Aminoethyl)-2-butyl-7-(pyridin-3-yl)-1H-imidazo[4,5-c]quinolin-4-amineHCID 21984422—
생성물N-{2-[4-amino-2-butyl-7-(pyridin-3-yl)-1H-imidazo[4,5-c]quinolin-1-yl]ethyl}-2-methylpropanamideHCID 2198424725.8%

반응 단계

1-(2-Aminoethyl)-2-butyl-7-(pyridin-3-yl)-1H-imidazo[4,5-c]quinolin-4-amine (2.00 g, 5.50 mmol) was treated with triethylamine (1.01 mL, 7.26 mmol) and isobutyryl chloride (0.64 mL, 6.10 mmol) according to the method described in Part B of Examples 372-376. The crude product was recrystallized from isopropanol (4 mL/g) and then triturated with acetonitrile (12.5 mL/g), isolated by filtration, and dried overnight in a drying oven to provide 0.61 g of N-{2-[4-amino-2-butyl-7-(pyridin-3-yl)-1H-imidazo[4,5-c]quinolin-1-yl]ethyl}-2-methylpropanamide as a white solid, mp 228-230° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07598382B2
출처 데이터셋uspto-grants-2009_10
ORD IDord-b771713d354542d6ac9e20cf48af0eef
출처 메모uspto-grants-2009_10