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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 249841생성일: 2026년 10월 26일

4-Aminopyridine → Methyl 2-(pyridin-4-ylamino)benzoxazole-4-carboxylate

https://huagongshe.com/reaction/249841

반응식

참여 물질

역할이름HCID투입량
반응물4-AminopyridineHCID 1727—
반응물Potassium CarbonateHCID 11430—
반응물2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenylHCID 11155794—
반응물Methyl 2-chlorobenzo[d]oxazole-4-carboxylateHCID 56924368—
촉매palladium(II) acetateHCID 167845—
용매tert-ButanolHCID 6386—
생성물Methyl 2-(pyridin-4-ylamino)benzoxazole-4-carboxylateHCID 66873583—

반응 조건

온도90 °C

반응 단계

A mixture of methyl 2-chlorobenzoxazole-4-carboxylate (350 mg, 1.65 mmol), 4-aminopyridine (233 mg, 2.48 mmol), palladium(II) acetate (7.4 mg, 0.033 mmol), 2-dicyclohexylphosphino-2′,4′,6′-triisopropylbiphenyl (39 mg, 0.083 mmol), K2CO3 (570 mg, 4.13 mmol) and t-BuOH (4 mL) was heated to 90° C. for 40 min. After cooling to room temperature, the reaction mixture was filtered through diatomaceous earth and concentrated. The crude product was purified by column chromatography (silica gel, 9:1 CH2Cl2/CH3OH) to afford methyl 2-(pyridin-4-ylamino)benzoxazole-4-carboxylate. 1H NMR and MS consistent.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07863271B2
출처 데이터셋uspto-grants-2011_01
ORD IDord-64aad37a3af54c31889d64be9c5b2f5a
출처 메모uspto-grants-2011_01