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HRID 81955作成日:2026年10月26日

Ethanesulfonylchloride, 2-chloro- → N-(2,6-diethylphenyl)-8-{[1-(ethenylsulfonyl)piperidin-4-yl]amino}-1-methyl-4,5-dihydro-1H-pyrazolo[4,3-h]quinazoline-3-carboxamide

https://huagongshe.com/reaction/81955

反応式

関与物質

役割名称HCID仕込み量
反応物Ethanesulfonylchloride, 2-chloro-HCID 15385—
反応物DiisopropylethylamineHCID 81531—
反応物N-(2,6-diethylphenyl)-1-methyl-8-(piperidin-4-ylamino)-4,5-dihydro-1H-pyrazolo[4,3-h]quinazoline-3-carboxamide hydrochlorideHCID 44555920—
溶媒DichloromethaneHCID 6344—
生成物N-(2,6-diethylphenyl)-8-{[1-(ethenylsulfonyl)piperidin-4-yl]amino}-1-methyl-4,5-dihydro-1H-pyrazolo[4,3-h]quinazoline-3-carboxamideHCID 6707590656%

反応条件

温度-78 °C

反応手順

To a solution of N-(2,6-diethylphenyl)-1-methyl-8-(piperidin-4-ylamino)-4,5-dihydro-1H-pyrazolo[4,3-h]quinazoline-3-carboxamide hydrochloride (300 mg, 0.606 mmol) under nitrogen, in dry dichloromethane (15 mL), DIPEA (0.527 mL, 3.03 mmol) and 300 mg of molecular sieves were added, and the mixture was cooled at −78° C. 2-chloroethanesulfonyl chloride (0.063 mL, 0.606 mmol) was added. Temperature was allow to rise to room temperature then the solvent was evaporated to dryness and the crude was purified by flash chromatography on silica gel (eluant: ethyl acetate/dichloromethane: 2/8) to give 185 mg of the title compound (56% yield).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08846701B2
出典データセットuspto-grants-2014_09
ORD IDord-929f571a356f4d6497886d33fd952cef
出典メモuspto-grants-2014_09