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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 515089생성일: 2026년 10월 27일

Methyl 4-aminopyridine-2-carboxylate → 4-(4,5-dichloro-2-(4-fluoro-2-methoxyphenoxy)benzamido)picolinic Acid

https://huagongshe.com/reaction/515089

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참여 물질

역할이름HCID투입량
반응물Methyl 4-aminopyridine-2-carboxylateHCID 3759117—
반응물Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
반응물4,5-Dichloro-2-(4-fluoro-2-methoxyphenoxy)benzoic acidHCID 90314379—
촉매Sodium HydroxideHCID 14798—
용매DimethylformamideHCID 6228—
생성물4-(4,5-dichloro-2-(4-fluoro-2-methoxyphenoxy)benzamido)picolinic AcidHCID 903154537%

반응 조건

온도50 °C

반응 단계

4,5-Dichloro-2-(4-fluoro-2-methoxy-phenoxy)benzoic acid (40 mg, 0.12 mmol), methyl 4-aminopicolinate (36.5 mg, 0.24 mmol) and HATU (45.9 mg, 0.12 mmol) were combined in DMF (1 mL) and heated at 50° c. for 2 hours. The reaction was treated with 10 drops of 3 M NaOH and heated at 50° C. for 16 h. The reaction was filtered and purified by reverse phase HPLC using a gradient of acetonitrile in water containing HCl (5 mM) as a modifier (10-99%) to yield 4-(4,5-dichloro-2-(4-fluoro-2-methoxyphenoxy)benzamido)picolinic acid (76) (3.80 mg, 7%). ESI-MS m/z calc. 450.02, found 451.1 (M+1)+; Retention time: 1.47 minutes (3 minutes run).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09108903B2
출처 데이터셋uspto-grants-2015_08
ORD IDord-e133735061df45b5a7dec9d5febd4b4e
출처 메모uspto-grants-2015_08