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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1828593생성일: 2026년 10월 25일

Cyclohexyl isocyanate → N-(Cyclohexyl)-4-(4-chlorophenyl)-5-(2,4-dichlorophenyl)-1-methylimidazole-2-carboxamide

https://huagongshe.com/reaction/1828593

반응식

참여 물질

역할이름HCID투입량
반응물Cyclohexyl isocyanateHCID 18502—
반응물4-(4-Chlorophenyl)-5-(2,4-dichlorophenyl)-1-methylimidazoleHCID 22066083—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
생성물N-(Cyclohexyl)-4-(4-chlorophenyl)-5-(2,4-dichlorophenyl)-1-methylimidazole-2-carboxamideHCID 10204999—

반응 단계

To a solution of 4-(4-chlorophenyl)-5-(2,4-dichlorophenyl)-1-methylimidazole (50 mg, 0.15 mmol) from Example 32, Step C in THF (3 mL) cooled to −70° C. in a dry ice/acetone bath was added 1.6N n-butyl lithium in hexanes (0.11 mL, 0.18 mmol). The reaction was stirred for 1 hr and then cyclohexyl isocyanate (0.040 mL, 30 mmol) was added via syringe. The reaction was allowed to warm to rt for 1 hr and was then quenched with aq. sodium bicarbonate and extracted twice with ethyl acetate. The organic layers were washed with brine, dried over sodium sulfate, and evaporated. The residue was purified by Prep TLC (1 mm, silica) (100% methylene chloride) to afford the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07057051B2
출처 데이터셋uspto-grants-2006_06
ORD IDord-e9a99b1ec7404786be72cf026a3b34fa
출처 메모uspto-grants-2006_06