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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 335310생성일: 2026년 10월 25일

Pyridine → Methyl 3-(7-bromoimidazo[1,2-a]pyridine-3-carboxamido)-4-methylbenzoate

https://huagongshe.com/reaction/335310

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물Thionyl ChlorideHCID 24386—
반응물Methyl 3-amino-4-methylbenzoateHCID 337778—
반응물3-[(7-Bromo-imidazo[1,2-a]pyridine-3-carbonyl)-amino]-4-fluorobenzoic acidHCID 71283443—
용매Ethyl AcetateHCID 8857—
생성물Methyl 3-(7-bromoimidazo[1,2-a]pyridine-3-carboxamido)-4-methylbenzoateHCID 71283103—

반응 단계

A mixture comprising 7-bromoimidazo[1,2-a]pyridine-3-carboxylic acid (Intermediate 1A step 3) (750 mg, 3.11 mmol) and thionyl chloride (5 ml, 68.5 mmol) under N2 was heated at reflux for 2 hrs. The mixture was concentrated in vacuo and azeotroped with toluene. Methyl 3-amino-4-methylbenzoate (514 mg, 3.11 mmol) (pre-dried at 45° C.) was added followed by pyridine (5 ml) and the mixture was stirred at room temperature under N2 overnight. The reaction mixture was diluted with EtOAc and washed with sat. NaHCO3, brine, H2O, dried (MgSO4) and concentrated in vacuo. Purification by chromatography on silica eluting with 50-100% EtOAc in iso-hexane afforded the title compound as an orange solid;

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08883819B2
출처 데이터셋uspto-grants-2014_11
ORD IDord-973abd30f88f43e5a53172b267f448f1
출처 메모uspto-grants-2014_11