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HRID 49862생성일: 2026년 10월 23일

4-Aminoacetanilide → 1-(4-Acetaminoanilino)-4-(4-pyridylmethyl)phthalazine

https://huagongshe.com/ko/reaction/49862

반응식

참여 물질

역할이름HCID투입량
반응물4-AminoacetanilideHCID 31230—
반응물1-Chloro-4-(4-pyridinylmethyl)phthalazineHCID 1944609—
용매1-ButanolHCID 263—
생성물1-(4-Acetaminoanilino)-4-(4-pyridylmethyl)phthalazineHCID 22741957—

반응 조건

온도110 °C

반응 단계

A mixture of 0.511 g (2 mmol) 1-chloro-4-(4-pyridylmethyl)phthalazine, 0.901 g (6 mmol) 4-aminoacetanilide and 5 ml 1-butanol is heated for 3 h at 110° C. The reaction mixture is then evaporated under vacuum, the crystalline residue is taken up in a mixture of 20 ml dichloromethane and 10 ml 20% aqueous potassium carbonate solution while stirring, then filtered and the filter residue washed with water and dichloromethane. After recrystallization from dichloromethane/methanol and drying under HV (8 h, 100° C.), title compound is obtained with a methanol content of 1.27%; m.p. >270° C.; 1H NMR (DMSO-d6) 9.91 (s, 1H), 9.13 (s, 1H), 8.59-8.64 (m, 1H), 8.48 (d, 2H), 8.08-8.13 (m, 1H), 7.91-8.01 (m, 2H), 7.85 (d, 2H), 7.58 (d, 2H), 7.32 (d, 2H), 4.58 (s, 2H), 2,05 (s, 3H), [methanol: 4.13 (q, 0.15H), 3.19 (d, 0.45H)]; ESI-MS: (M+H)+=370.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06710047B2
출처 데이터셋uspto-grants-2004_03
ORD IDord-00f06d4ab1d24d15b267718d87e9d089
출처 메모uspto-grants-2004_03