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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 47347생성일: 2026년 10월 24일

Ammonia → 1-(3-Amino-3-methyl-1-butynyl)-4-[(3-chloro-4-methoxybenzyl)amino]-6-phthalazinecarbonitrile hydrochloride

https://huagongshe.com/ko/reaction/47347

반응식

참여 물질

역할이름HCID투입량
반응물AmmoniaHCID 222—
반응물TriethylamineHCID 8471—
반응물3-Butyn-2-amine, 2-methyl-HCID 76319—
반응물1-Chloro-4-((3-chloro-4-methoxybenzyl)amino)-6-phthalazinecarbonitrileHCID 10451065—
촉매HCID 178418476HCID 178418476—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물1-(3-Amino-3-methyl-1-butynyl)-4-[(3-chloro-4-methoxybenzyl)amino]-6-phthalazinecarbonitrile hydrochlorideHCID 2274449972.4%

반응 조건

온도80 °C

반응 단계

0.39 ml triethylamine was added to a mixture of 500 mg 1-chloro-4-[(3-chloro-4-methoxybenzyl)amino]-6-phthalazine carbonitrile, 53 mg cuprous iodide, 98 mg dichlorobis(triphenylphosphine)palladium (II), 347 mg 3-amino-3-methyl-1-butyne, and 10 ml dimethylformamide, and the mixture was stirred at 80° C. for 3 hr in a nitrogen atmosphere. After cooling, ethyl acetate was added to the reaction solution, then water and conc. aqueous ammonia were added thereto, and the organic layer was recovered. The organic layer was washed with dilute aqueous ammonia and brine, and dried over anhydrous sodium sulfate. It was filtered and the filtrate was evaporated. The resulting residue was purified by NH-form silica gel column chromatography to give 446 mg of the title compound. The product was converted in a usual manner into the hydrochloride.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06699870B2
출처 데이터셋uspto-grants-2004_03
ORD IDord-2d8b3da9fef948209fab9deea4af6ff3
출처 메모uspto-grants-2004_03