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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 16726생성일: 2026년 10월 24일

Oxalyl chloride → HCID 178480676, 화합물

https://huagongshe.com/ko/reaction/16726

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참여 물질

역할이름HCID투입량
반응물Oxalyl chlorideHCID 65578—
반응물DiisopropylethylamineHCID 81531—
반응물4-(4-Methylpiperazin-1-yl)benzoic acidHCID 736532—
반응물5-(2-Phenylethyl)-1H-pyrazol-3-amineHCID 178507523—
촉매DichloromethaneHCID 6344—
용매DichloromethaneHCID 6344—
생성물HCID 178480676HCID 1784806764.6%

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온도0 °C

반응 단계

Oxalyl chloride (2M in DCM, 250 μl, 0.50 mmol, 1.1 eq) was added dropwise to a mixture of 4-(4-methylpiperazin-1-yl)benzoic acid (100 mg, 0.45 mmol, 1 eq) in DCM (5 ml, containing a few drops of DMF) and DIPEA (171 μl, 0.95 mmol, 2.1 eq) at O° C. After stirring for 1 h at 0° C., a solution of 5-phenethyl-2H-pyrazol-3-amine (128 mg, 0.68 mmol, 1.5 eq) in DCM (2 ml) was added dropwise. The mixture was maintained at 0° C. for 2 h, then gradually allowed to warm to room temperature overnight. The mixture was diluted with DCM (50 ml), washed with aq. NaHCO3 solution (50 ml) and the aqueous layer was extracted with DCM (50 ml). The combined organic layers were concentrated. The crude product was purified by reverse-phase prep. HPLC (basic) using a 30-50% gradient of acetonitrile in water (containing 1% ammonium hydroxide) to yield the title compound (8 mg, 3% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07737149B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-497ee524cd6c46a081af0d4567cf7fca
출처 메모uspto-grants-2010_06