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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 9437생성일: 2026년 10월 24일

Isopropyl isocyanate → N-{2-[4-amino-2-ethoxymethyl-7-(pyridin-3-yl)-1H-imidazo[4,5-c]quinolin-1-yl]ethyl}-N'-(1-methylethyl)urea

https://huagongshe.com/ko/reaction/9437

반응식

참여 물질

역할이름HCID투입량
반응물Isopropyl isocyanateHCID 61277—
반응물1-(2-Aminoethyl)-2-ethoxymethyl-7-(pyridin-3-yl)-1H-imidazo[4,5-c]quinolin-4-amineHCID 21984105—
용매ChloroformHCID 6212—
생성물N-{2-[4-amino-2-ethoxymethyl-7-(pyridin-3-yl)-1H-imidazo[4,5-c]quinolin-1-yl]ethyl}-N'-(1-methylethyl)ureaHCID 2198429728.5%

반응 단계

A solution of 1-(2-aminoethyl)-2-ethoxymethyl-7-(pyridin-3-yl)-1H-imidazo[4,5-c]quinolin-4-amine (2.50 g, 6.90 mmol) in chloroform (50 mL) was treated with isopropyl isocyanate (0.65 mL, 6.9 mmol) according to the method described in Examples 377–379. The crude product was purified by column chromatography on silica gel (eluting with 94:6 chloroform:methanol) followed by trituration with acetonitrile (15 mL/g) at 95° C. The mixture was cooled in an ice bath, isolated by filtration, and dried for one hour in a vacuum oven at 100° C. to provide 0.88 g of N-{2-[4-amino-2-ethoxymethyl-7-(pyridin-3-yl)-1H-imidazo[4,5-c]quinolin-1-yl]ethyl}-N′-(1-methylethyl)urea as a white solid, mp 194–196° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07091214B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-d16d8d902d0c45cfb7ea9fa85a26dbda
출처 메모uspto-grants-2006_08