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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 405791생성일: 2026년 10월 25일

Oxalyl chloride → N-(5-cyano-2-methylphenyl)-6-fluoroimidazo[1,2-a]pyridine-3-carboxamide

https://huagongshe.com/reaction/405791

반응식

참여 물질

역할이름HCID투입량
반응물Oxalyl chlorideHCID 65578—
반응물DiisopropylethylamineHCID 81531—
반응물3-Amino-4-methylbenzonitrileHCID 7016428—
반응물6-Fluoroimidazo[1,2-a]pyridine-3-carboxylic acidHCID 55268195—
용매1,2-DichloroethaneHCID 11—
용매DimethylformamideHCID 6228—
용매DichloromethaneHCID 6344—
생성물N-(5-cyano-2-methylphenyl)-6-fluoroimidazo[1,2-a]pyridine-3-carboxamideHCID 71280520—

반응 조건

온도60 °C

반응 단계

Oxalyl chloride (10 mL, 110 mmol) was added dropwise to a stirred suspension of 6-fluoroimidazo[1,2-a]pyridine-3-carboxylic acid (24b) (2 g, 11 mmol) and catalytic amounts of DMF in dichloromethane (20 mL). After 5 hours, the solvent was evaporated and the solid was suspended in dry DCE (20 mL) and added to a stirred solution of 3-amino-4-methylbenzonitrile (1.45 g, 11 mmol) and DIEA (6 mmol) in DCE (10 mL) at 0° C. After the addition, the reaction was heated at 60° C. for 5 hours. The mixture was subjected to standard aqueous work and silica purification to give N-(5-cyano-2-methylphenyl)-6-fluoroimidazo[1,2-a]pyridine-3-carboxamide (39) as a solid. 1H NMR (400 MHz, d6-DMSO) δ 10.14 (s, 1H), 9.45 (dd, J=5.2, 2.0 Hz, 1H), 8.62 (s, 1H), 7.90-7.87 (m, 2H), 7.68-7.63 (m, 1H), 7.53 (d, J=8.0 Hz, 1H), 2.37 (s, 3H). MS m/z 295.1 (M+1)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08754071B2
출처 데이터셋uspto-grants-2014_06
ORD IDord-079cc8e77ea7476f8039defd36e3b38b
출처 메모uspto-grants-2014_06