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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1246779생성일: 2026년 10월 24일

2,4-Dichlorobenzoyl chloride → 2,4-dichloro-N-[4-chloro-6-(4-chlorophenylamino)-pyrimidin-5-yl]-benzamide

https://huagongshe.com/ko/reaction/1246779

반응식

참여 물질

역할이름HCID투입량
반응물2,4-Dichlorobenzoyl chlorideHCID 66645—
반응물6-Chloro-N4-(4-chlorophenyl)pyrimidine-4,5-diamineHCID 16726311—
용매PyridineHCID 1049—
생성물2,4-dichloro-N-[4-chloro-6-(4-chlorophenylamino)-pyrimidin-5-yl]-benzamideHCID 21905838—

반응 단계

6-Chloro-N4-(4-chlorophenyl)-pyrimidine-4,5-diamine I-(1A-1)a (34 g, 134 mmol) in pyridine (150 ml) was cooled to 0° C. and to it was added 2,4-dichlorobenzoyl chloride (25 ml, 178 mmol). The reaction was allowed to warm to ambient temperature overnight. The solid precipitate was collected by vacuum filtration and dried under high vacuum to yield the title compound I-(1A-1)b as a colorless solid (14 g, 25%). The pyridine solution was concentrated under reduced pressure and then triturated with methanol (500 ml) to provide additional material (35 g, 60%): +ESI MS (M+1) 427.4; 1H NMR: (400 MHz, DMSO-d6): δ 10.08 (s, 1H), 9.16 (s, 1H), 8.38 (s, 1H), 7.97 (d, J=8.7 Hz, 1H), 7.75 (d, J=2.0 Hz, 2H), 7.64–7.60 (m, 3H), 7.40 (d, J=8.7 Hz, 2H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07129239B2
출처 데이터셋uspto-grants-2006_10
ORD IDord-2e84fe40d4d7488f8d26f2bb1084dfd2
출처 메모uspto-grants-2006_10