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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 49863생성일: 2026년 10월 24일

1-Phenethylamine, (-)- → (S)-1-(1-Phenylethylamino)-4-(4-pyridylmethyl)phthalazine

https://huagongshe.com/ko/reaction/49863

반응식

참여 물질

역할이름HCID투입량
반응물1-Phenethylamine, (-)-HCID 75818—
반응물1-Chloro-4-(4-pyridinylmethyl)phthalazineHCID 1944609—
용매1-ButanolHCID 263—
생성물(S)-1-(1-Phenylethylamino)-4-(4-pyridylmethyl)phthalazineHCID 54550094—

반응 조건

온도110 °C

반응 단계

A mixture of 0.511 g (2 mmol) 1-chloro-4-(4-pyridylmethyl)phthalazine, 1.273 ml (10 mmol) (S)-1 phenylethylamine and 5 ml 1-butanol is stirred for 24 h at 110° C. The reaction mixture is evaporated under vacuum and the residue distributed between dichloromethane and 20% aqueous potassium carbonate solution. The organic phase dried over anhydrous sodium sulfate is evaporated in the RE and then under HV and the residue purified on silica gel by flash chromatography using dichloromethane/methanol (50:1). The product-containing fractions are dissolved in 5 ml methanol, acidified with 0.75 ml 3N methanolic HCl and evaporated under vacuum. After recrystallization of the residue from methanol/acetonitrile, drying of the crystallizate under HV (8 h, 100° C.) and equilibration for 15 h at 20° C. and in room atmosphere, title compound is obtained with a water content of 10.66%; m.p. 190° C. (decomp.); ESI-MS: (M+H)+=341; [α]D20 =+42.1±0.8° (c=1.272%, methanol).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06710047B2
출처 데이터셋uspto-grants-2004_03
ORD IDord-aba9693d37aa4c728072a9adba9d472f
출처 메모uspto-grants-2004_03