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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 49891생성일: 2026년 10월 25일

4-Aminobiphenyl → N-(4-phenylphenyl)-4-(pyridin-4-ylmethyl)phthalazin-1-amine

https://huagongshe.com/reaction/49891

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참여 물질

역할이름HCID투입량
반응물4-AminobiphenylHCID 7102—
반응물Triethylamine hydrochlorideHCID 11130—
반응물Phosphorus oxide (P4O10)HCID 14812—
반응물Carbonate IonHCID 19660—
반응물4-(4-Pyridylmethyl)-1(2H)-phtalazinoneHCID 789954—
용매WaterHCID 962—
용매Dichloromethane methanolHCID 21226129—
생성물N-(4-phenylphenyl)-4-(pyridin-4-ylmethyl)phthalazin-1-amineHCID 6419389—

반응 조건

온도200 °C

반응 단계

A mixture of 2.41 g (16.98 mmol) phosphorus pentoxide, 2.32 g (16.85 mmol) triethylamine hydrochloride, 3 g (17.73 mmol) 4-aminobiphenyl, and 1 g (4.21 mmol) 4-(4-pyridylmethyl)-1(2H)-phthalazinone is stirred for 20 h at 200° C. under a nitrogen atmosphere. After cooling to RT, the hyalinocrystalline melt is distributed between a dichloromethane/methanol mixture (99:1) and a mixture of water and saturated aqueous carbonate solution on (1:1) with intensive stirring and the use of an ultrasonic bath. The organic phase dried over sodium sulfate is evaporated under vacuum and the residue purified by means of flash chromatography on silica gel with particle size 0.04-0.06 mm, using a dichloromethane/methanol mixture (49:1). Title compound is obtained after evaporation of the product-containing fractions under vacuum and recrystallization of the residue from acetonitrile; m.p. 189-191 °C.; ESI-MS: (M+H)+=389.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06710047B2
출처 데이터셋uspto-grants-2004_03
ORD IDord-68d8d685ff174f3fb8764293eccc5175
출처 메모uspto-grants-2004_03