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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 49885생성일: 2026년 10월 25일

Ammonia → 1-(3-Methylanilino)-4-(4-pyridylmethyl)phthalazine

https://huagongshe.com/reaction/49885

반응식

참여 물질

역할이름HCID투입량
반응물AmmoniaHCID 222—
반응물m-ToluidineHCID 7934—
반응물Triethylamine hydrochlorideHCID 11130—
반응물TetramethylureaHCID 12437—
반응물Phosphorus oxide (P4O10)HCID 14812—
반응물4-(4-Pyridylmethyl)-1(2H)-phtalazinoneHCID 789954—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
생성물1-(3-Methylanilino)-4-(4-pyridylmethyl)phthalazineHCID 6419387—

반응 조건

온도200 °C

반응 단계

A mixture of 2.39 g (16.8 mmol) phosphorus pentoxide, 2.31 g (16.8 mmol) triethylamine hydrochloride, and 1.82 ml (16.8 mmol) m-toluidine is heated and stirred in a nitrogen atmosphere at 200° C. until a homogeneous melt has formed. To the melt, 1 g (4.2 mmol) 4-(4-pyridylmethyl)-1(2H)-phthalazinone is added and the reaction mixture stirred for a further 3.5 h at 205° C. After cooling to about 170° C., 4 ml tetramethylurea is added to the reaction mixture, followed by 2 ml water at about 110° C. The mixture is stirred for a further 30 min while cooling to RT and then distributed between dichloromethane and a mixture of 20 ml water and 5 ml conc. ammonia. The organic phase dried over sodium sulfate is concentrated by evaporation and the residue purified on silica gel by flash chromatography using acetate and acetate/methanol (99:1 and 19:1). Title compound is obtained after crystallization of the product-containing fractions from acetonitrile and subsequent recrystallization from acetate; m.p. 141-143° C.; ESI-MS: (M+H)+=327.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06710047B2
출처 데이터셋uspto-grants-2004_03
ORD IDord-2d57d14ff339450ebd4864938eadbeb0
출처 메모uspto-grants-2004_03