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HRID 1770402作成日:2026年10月25日

Triethylamine → HCID 67242423、化合物

https://huagongshe.com/reaction/1770402

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Oxalyl chlorideHCID 65578—
反応物Sodium BicarbonateHCID 516892—
反応物3,5-Bis(difluoromethyl)-1H-pyrazole-1-acetic acidHCID 1229844—
反応物HCID 67238250HCID 67238250—
触媒DimethylformamideHCID 6228—
溶媒DichloromethaneHCID 6344—
生成物HCID 67242423HCID 67242423—

反応手順

To a solution of [3,5-bis-(difluoromethyl)-1H-pyrazol-1-yl]acetic acid (177 mg) in dichloromethane (40 ml) are added, at 0° C., oxalyl chloride (290 mg) and one drop of N,N-dimethylformamide. The reaction mixture is stirred at room temperature for 2 hours. The solvent and the excess reagent are removed under reduced pressure. The solid residue is again dissolved in dichloromethane and, at 0° C., added dropwise to a solution of 4-{4-[5-(2-chloro-6-hydroxyphenyl)-4,5-dihydro-1,2-oxazol-3-yl]-1,3-thiazol-2-yl}piperidinium chloride and triethylamine (5.0 eq.) in dichloromethane (25 ml). The reaction mixture is stirred at room temperature overnight. Then it is admixed with concentrated sodium hydrogencarbonate solution, and the aqueous phase is removed and extracted with ethyl acetate. The combined organic phases are dried over sodium sulphate and concentrated. Purification by column chromatography gives 2-[3,5-bis(difluoromethyl)-1H-pyrazol-1-yl]-1-(4-{4-[5-(2-chloro-6-hydroxyphenyl)-4,5-dihydro-1,2-oxazol-3-yl]-1,3-thiazol-2-yl}piperidin-1-yl)ethanone (110 mg).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09247748B2
出典データセットuspto-grants-2016_02
ORD IDord-a164863e395a40cb8e57581520960bd8
出典メモuspto-grants-2016_02