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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 16737생성일: 2026년 10월 23일

4-Fluorobenzoic Acid → HCID 178489757, 화합물

https://huagongshe.com/ko/reaction/16737

반응식

참여 물질

역할이름HCID투입량
반응물4-Fluorobenzoic AcidHCID 9973—
반응물Oxalyl chlorideHCID 65578—
반응물DiisopropylethylamineHCID 81531—
반응물HCID 178489815HCID 178489815—
촉매DimethylformamideHCID 6228—
용매DichloromethaneHCID 6344—
생성물HCID 178489757HCID 1784897573%

반응 조건

온도0 °C

반응 단계

Oxalyl chloride (2M in DCM, 1.40 ml, 2.75 mmol, 1.1 eq) was added dropwise to a mixture of 4-fluorobenzoic acid (350 mg, 2.50 mmol, 1 eq) in dichloromethane (15 ml) at 0° C. containing a few drops of DMF (10 ul, 0.12 mmol, 0.05 eq) and DIPEA (937 μl, 5.25 mmol, 2.1 eq). After stirring for 60 mins at 0° C. a solution of 5-[2-(3,5-dimethoxyphenyl)ethyl]-2H-pyrazol-3-amine (742 mg, 3 mmol, 1.2 eq) in DCM (10 ml) was added dropwise over 15 mins. The mixture was maintained at 0° C. for a further 2 h, then gradually allowed to warm to room temperature overnight. The mixture was diluted with DCM (50 ml) and washed with aqueous NaHCO3 solution (50 ml). The aqueous layer was extracted with DCM (50 ml). The combined organic layers were collected and concentrated. The crude product was purified by reverse-phase prep HPLC using a 30-50% gradient of acetonitrile in water containing 1% ammonium hydroxide solution. The desired fractions were evaporated to afford the title compound as a beige solid. (31.5 mg, 3% yield)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07737149B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-1e71506f710044cbbbadcf5045c78d46
출처 메모uspto-grants-2010_06