돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1271031생성일: 2026년 10월 27일

Benzene, 1-chloro-4-ethynyl- → 4-Chloro-5-(4-chlorophenylethynyl)-2-diisopropylaminomethyleneaminopyrimidine

https://huagongshe.com/reaction/1271031

반응식

참여 물질

역할이름HCID투입량
반응물Benzene, 1-chloro-4-ethynyl-HCID 70118—
반응물4-Chloro-2-diisopropylaminomethyleneamino-5-iodopyrimidineHCID 73446451—
촉매Copper iodideHCID 83717—
촉매HCID 178418476HCID 178418476—
용매TriethylamineHCID 8471—
생성물4-Chloro-5-(4-chlorophenylethynyl)-2-diisopropylaminomethyleneaminopyrimidineHCID 7344644994.7%

반응 단계

A mixture of 0.722 g 4-chloro-2-diisopropylaminomethyleneamino-5-iodopyrimidine, 3.5 mL triethylamine, 0.025 g copper iodide, 0.037 g dichlorobis(triphenyl)phosphine palladium II and 0.289 g 1-chloro-4-ethynylbenzene was stirred under nitrogen at room temperature for 18 hours. The dark brown mixture was evaporated in vacuo at a bath temperature of 30–35° C. The beige residue was partitioned between dichloromethane and water. The organic phase was washed twice with water, dried over sodium sulfate, filtered and evaporated to yield 1.0 g of a caramel colored film. The residue was dissolved in 1:1 dichloromethane/hexanes and purified by column chromatography on silica gel, eluting successively with 1:1 dichloromethane/hexanes, dichloromethane and ethyl acetate. The product was recovered from the latter two eluates by evaporation to yield 0.7 g of 4-chloro-5-(4-chlorophenylethynyl)-2-diisopropylaminomethyleneaminopyrimidine.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07205297B2
출처 데이터셋uspto-grants-2007_04
ORD IDord-5f70233f91a747e5ae1790c09c11c6e5
출처 메모uspto-grants-2007_04