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HRID 1371992作成日:2026年10月25日

Propylphosphonic anhydride → 4-[2-(4-Chloro-5 methyl-3-trifluoromethyl-pyrazol-1yl)-acetyl]-piperazine-1carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/1371992

反応式

関与物質

役割名称HCID仕込み量
反応物Propylphosphonic anhydrideHCID 111923—
反応物tert-Butyl piperazine-1-carboxylateHCID 143452—
反応物(4-Chloro-5-methyl-3-trifluoromethyl-pyrazol-1-yl)-acetic acidHCID 1876853—
溶媒DichloromethaneHCID 6344—
生成物4-[2-(4-Chloro-5 methyl-3-trifluoromethyl-pyrazol-1yl)-acetyl]-piperazine-1carboxylic acid tert-butyl esterHCID 5949228946.9%

反応条件

温度0 °C

反応手順

(4-Chloro-5-methyl-3-trifluoromethyl-pyrazol-1-yl)-acetic acid (1.5 g, 6.18 mmol) was taken in dry DCM (20 mL) and cooled to 0° C. To this cold mixture was added N-boc piperazine (1.15 g, 6.18 mmol) followed by addition of T3P (8 g, 12.4 mmol, 50% solution in EtOAc). The reaction was left overnight at rt. The mixture was diluted with CH2Cl2, washed with NaHCO3 soln, brine, dried (Na2SO4) and concentrated to afford the crude product that was washed thoroughly with ether-pet ether to afford 4-[2-(4-Chloro-5 methyl-3-trifluoromethyl-pyrazol-1yl)-acetyl]-piperazine-1carboxylic acid tert-butyl ester (1.2 g, 2.9 mmol). This was dissolved in methanol (25 mL) cooled to 0° C. and HCl saturated ether (3 mL) was added to it. The mixture was stirred at room temperature for 4 h and concentrated. Crystallization from MeOH/Petroleum ether yielded product.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07157464B2
出典データセットuspto-grants-2007_01
ORD IDord-7c58ef2faee84f9a96e3be8583935d20
出典メモuspto-grants-2007_01