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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 133106생성일: 2026년 10월 25일

4-Pyridinecarboxaldehyde → 2-(4-tert-butyl-phenyl)-8-[(pyridin-4-ylmethyl)-amino]-2H-phthalazin-1-one

https://huagongshe.com/reaction/133106

반응식

참여 물질

역할이름HCID투입량
반응물4-PyridinecarboxaldehydeHCID 13389—
반응물P-ToluenesulfonylhydrazideHCID 15303—
반응물Sodium triacetoxyborohydrideHCID 5049666—
반응물8-amino-2-(4-tert-butyl-phenyl)-2H-phthalazin-1-oneHCID 69160627—
용매DichloromethaneHCID 6344—
생성물2-(4-tert-butyl-phenyl)-8-[(pyridin-4-ylmethyl)-amino]-2H-phthalazin-1-oneHCID 11406487—

반응 단계

To a solution of the amine (Step E, 45 mg, 0.15 mmol) and CH2Cl2 (10 mL) was added 4-pyridinecarboxaldehyde (0.04 mL, 0.39 mmol) and NaBH(OAc)3 (95 mg, 0.45 mmol). The reaction was stirred at RT for 7 h then quenched with H2O and extracted with CH2Cl2. The organic layer was washed with H2O and brine, dried (MgSO4) and concentrated in vacuo to give the crude product as an orange oil. The crude product was dissolved in 10 mL CH2Cl2 and stirred with PS-TsNHNH2 resin to remove un-reacted aldehyde. After 1 h, the mixture was filtered through Celite® and concentrated in vacuo. The residue was purified by silica flash chromatography (20-75% EtOAc:hexane) to give the desired product as a light-yellow crystalline solid. MS m/e 385 (M+H)+. Calc'd for C24H24N4O-384.47.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07390820B2
출처 데이터셋uspto-grants-2008_06
ORD IDord-f5fd2b5e61724521a6e8851896d5c524
출처 메모uspto-grants-2008_06