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HRID 1641458作成日:2026年10月27日

Hydrochloric Acid → 3-bromo-N-(4-chloro-2-(1-cyclopropylethylcarbamoyl)phenyl)-1-(3-chloropyridin-2-yl)-1H-pyrazole-5-carboxamide

https://huagongshe.com/reaction/1641458

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物Potassium tert-butoxideHCID 23665647—
反応物2-amino-5-chloro-N-(1-cyclopropylethyl)benzamideHCID 43533096—
反応物phenyl 3-bromo-1-(3-chloropyridin-2-yl)-1H-pyrazole-5-carboxylateHCID 66737070—
溶媒Dimethyl SulfoxideHCID 679—
生成物3-bromo-N-(4-chloro-2-(1-cyclopropylethylcarbamoyl)phenyl)-1-(3-chloropyridin-2-yl)-1H-pyrazole-5-carboxamideHCID 6673619338.6%

反応手順

0.18 g of potassium tert-butoxide was added to a mixed solution comprising 0.23 g of 2-amino-5-chloro-N-(1-cyclopropylethyl)benzamide, 0.30 g of phenyl 3-bromo-1-(3-chloropyridin-2-yl)-1H-pyrazole-5-carboxylate and 5 ml of dimethyl sulfoxide, followed by reaction at room temperature for 1 hour. The reaction liquid was slowly added to diluted hydrochloric acid, the mixed liquid was subjected to extraction with ethyl acetate, and the organic layer was washed with a saturated sodium hydrogen carbonate aqueous solution and with a sodium chloride aqueous solution and dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure, and the residue was purified by silica gel column chromatography (eluent: n-hexane/ethyl acetate=8/2 to 7.5/2.5) to obtain 0.16 g of the desired product.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08115006B2
出典データセットuspto-grants-2012_02
ORD IDord-5c7e743ed5b64bc7bde86b38793f0962
出典メモuspto-grants-2012_02