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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1818185생성일: 2026년 10월 27일

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

https://huagongshe.com/reaction/1818185

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Isobutyryl chlorideHCID 62325—
반응물1-(2-Aminoethyl)-2-ethoxymethyl-7-(pyridin-3-yl)-1H-imidazo[4,5-c]quinolin-4-amineHCID 21984105—
생성물N-{2-[4-amino-2-ethoxymethyl-7-(pyridin-3-yl)-1H-imidazo[4,5-c]quinolin-1-yl]ethyl}-2-methylpropanamideHCID 2198403932.8%

반응 단계

1-(2-Aminoethyl)-2-ethoxymethyl-7-(pyridin-3-yl)-1H-imidazo[4,5-c]quinolin-4-amine (2.00 g, 5.50 mmol) was treated with triethylamine (1.00 mL, 7.20 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 93:7 acetonitrile:water and then from isopropanol (7.3 mL/g) and dried for two hours in a drying oven to provide 0.78 g of N-{2-[4-amino-2-ethoxymethyl-7-(pyridin-3-yl)-1H-imidazo[4,5-c]quinolin-1-yl]ethyl}-2-methylpropanamide as a white solid, mp 213-215° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07598382B2
출처 데이터셋uspto-grants-2009_10
ORD IDord-767c9f2ec926438ca93b53be004f7c7e
출처 메모uspto-grants-2009_10