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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 7792생성일: 2026년 10월 23일

Benzophenone imine → 6-[4-(1,3-benzoxazol-2-yl)-2-methoxyphenyl]-N-(diphenylmethylene)pyridin-3-amine

https://huagongshe.com/ko/reaction/7792

반응식

참여 물질

역할이름HCID투입량
반응물Benzophenone imineHCID 136809—
반응물2-(Dicyclohexylphosphino)biphenylHCID 2734216—
반응물2-[4-(5-Chloropyridin-2-yl)-3-methoxyphenyl]-1,3-benzoxazoleHCID 10308751—
반응물Sodium t-butoxideHCID 23676156—
촉매Bis(dibenzylideneacetone)palladiumHCID 9811564—
생성물6-[4-(1,3-benzoxazol-2-yl)-2-methoxyphenyl]-N-(diphenylmethylene)pyridin-3-amineHCID 21990952—

반응 조건

온도80 °C

반응 단계

2-[4-(5-chloropyridin-2-yl)-3-methoxyphenyl]-1,3-benzoxazole (100 mg, 0.30 mmol), benzophenone imine (60 μL, 0.36 mmol), Pd2(dba)3 (15 mg, 0.015 mmol), 1,1′-biphenyl-2-yl(dicyclohexyl)phosphine (10 mg, 0.015 mmol), NaOtBu (40 mg, 0.42 mmol) were combined in a sealable tube evacuated and backfilled with argon. Toluene (600 μL) was added and the mixture was degassed with a stream of argon for 5 min. The tube was sealed and the mixture was heated to 80° C. for 24 h. Crude mixture was adsorbed onto silica gel and purified by automated flash chromatography using an EtOAc/hexanes gradient to afford 6-[4-(1,3-benzoxazol-2-yl)-2-methoxyphenyl]-N-(diphenylmethylene)pyridin-3-amine as a yellow solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07087601B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-51f0adc9d41543e1b9f0d008ab664d0d
출처 메모uspto-grants-2006_08