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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 219940생성일: 2026년 10월 25일

4-(2-Methylpiperidin-1-yl)-3-nitrobenzoic acid → Methyl 2-fluoro-4-{5-[4-(2-methylpiperidin-1-yl)-3-nitrophenyl]-1,2,4-oxadiazol-3-yl}benzoate

https://huagongshe.com/reaction/219940

반응식

참여 물질

역할이름HCID투입량
반응물4-(2-Methylpiperidin-1-yl)-3-nitrobenzoic acidHCID 43176702—
반응물Methyl 4-[amino(hydroxyimino)methyl]-2-fluorobenzoateHCID 76644654—
용매TolueneHCID 1140—
용매DichloromethaneHCID 6344—
생성물Methyl 2-fluoro-4-{5-[4-(2-methylpiperidin-1-yl)-3-nitrophenyl]-1,2,4-oxadiazol-3-yl}benzoateHCID 67528992—

반응 단계

Intermediate 11 (12.46 g; 47.13 mmol) was dissolved in DCM (200 mL) and n,n′-dicyclohexylcarbodiimide (11.67 g; 56.56 mmol) was added. Then Intermediate 1 was added (10 g; 47.13 mmol) and the suspension was stirred at RT for 12 hours. The precipitate was filtered off and the solvent evaporated to give a yellow solid. The residue was dissolved in Toluene (300 mL) and Py (150 mL) and the solution was heated to 130° C. for 12 hours. The reaction mixture was concentrated to afford a yellow sticky oil which was precipitated from ACN affording the title compound as a yellow solid. LC/MS (Method B): 441.3 (M+H)+ HPLC: Rt 5.86 min (Purity: 95.1%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08202865B2
출처 데이터셋uspto-grants-2012_06
ORD IDord-0df5dd627ccf4d15b4245c25d38afc26
출처 메모uspto-grants-2012_06