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HRID 7668作成日:2026年10月24日

Sodium Hydroxide → 2-(4-Fluorophenyl)-1-[4-methoxy-2-(2-methylsulfanyl-pyrimidine-4-carbonyl)pyrazolidine-1-yl]-ethanone

https://huagongshe.com/ja/reaction/7668

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium HydroxideHCID 14798—
反応物2-(4-Fluorophenyl)-1-(4-methoxy-pyrazolidin-1-yl)-ethanoneHCID 21992191—
反応物2-Methylsulfonyl-pyrimidine-4-carbonyl chlorideHCID 21992194—
溶媒DichloromethaneHCID 6344—
溶媒Sodium CarbonateHCID 10340—
生成物2-(4-Fluorophenyl)-1-[4-methoxy-2-(2-methylsulfanyl-pyrimidine-4-carbonyl)pyrazolidine-1-yl]-ethanoneHCID 21992182—

反応手順

2-(4-Fluorophenyl)-1-(4-methoxy-pyrazolidin-1-yl)-ethanone, 47, (7.67 g, 32.2 mmol) and 2-methylsulfonyl-pyrimidine-4-carbonyl chloride (9.11 g, 48.3 mmol) are dissolved in dichloromethane (150 mL). A 0.5 N aqueous solution of sodium hydroxide (150 mL) is added steadily via addition funnel and the mixture is stirred vigorously at room temperature for 4 hours. The reaction is diluted with 5% aqueous sodium carbonate solution (1 L). The mixture is extracted with dichloromethane (6×200 mL). The combined organic layers are dried over magnesium sulfate, filtered and concentrated to give a red oil. The crude material is purified by over silica (1:1 to 1:3 hexane/ethyl acetate to 100% ethyl acetate) to afford 10.3 g of the desired product as a brown, viscous oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07087615B2
出典データセットuspto-grants-2006_08
ORD IDord-6940eccead1d4814aab7d5708d0adac2
出典メモuspto-grants-2006_08