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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 49859생성일: 2026년 10월 24일

4-Chloroaniline → 1-(4-Chloroanilino)-4-(4-pyridylmethyl)phthalazine hydrochloride

https://huagongshe.com/ko/reaction/49859

반응식

참여 물질

역할이름HCID투입량
반응물4-ChloroanilineHCID 7812—
반응물1-Chloro-4-(4-pyridinylmethyl)phthalazineHCID 1944609—
용매1-ButanolHCID 263—
생성물1-(4-Chloroanilino)-4-(4-pyridylmethyl)phthalazine hydrochlorideHCID 9886292—

반응 단계

A mixture of 1.28 g (5 mmol) 1-chloro-4-(4-pyridylmethyl)phthalazine, 0.67 g (5.25 mmol) 4-chloroaniline and 15 ml 1-butanol is heated for 0.5 h at 100 h while stirring in a nitrogen atmosphere. The mixture is then cooled to RT, filtered, and the filtrate washed with 1-butanol and ether. For purification, the crystallizate is dissolved in 40 ml of hot methanol, the solution treated with activated carbon, filtered via Hyflo Super Cel, and the filtrate evaporated to about half its original volume, resulting in the formation of a crystalline precipitate. After cooling to 0° C., filtration, washing of the filter residue with ether, and drying under HV for 8 h at 130° C., the title compound is obtained; m.p. >270° C.; 1H NMR (DMSO-d6) 9.80-11.40 (br), 8.89-8.94 (m, 1H), 8.67 (d, 2H), 8.25-8.30 (m, 1H), 8.06-8.17 (m, 2H), 7.87 (d, 2H), 7.69 (d, 2H), 7.49 (d, 2H), 4.81 (s, 2H); ESI-MS: (M+H)+=347.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06710047B2
출처 데이터셋uspto-grants-2004_03
ORD IDord-a9a371c157ff4e519c612c2e0a5f8130
출처 메모uspto-grants-2004_03