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HRID 16726作成日:2026年10月26日

Oxalyl chloride → HCID 178480676、化合物

https://huagongshe.com/reaction/16726

反応式

関与物質

役割名称HCID仕込み量
反応物Oxalyl chlorideHCID 65578—
反応物DiisopropylethylamineHCID 81531—
反応物4-(4-Methylpiperazin-1-yl)benzoic acidHCID 736532—
反応物5-(2-Phenylethyl)-1H-pyrazol-3-amineHCID 178507523—
触媒DichloromethaneHCID 6344—
溶媒DichloromethaneHCID 6344—
生成物HCID 178480676HCID 1784806764.6%

反応条件

温度0 °C

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07737149B2
出典データセットuspto-grants-2010_06
ORD IDord-497ee524cd6c46a081af0d4567cf7fca
出典メモuspto-grants-2010_06