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HRID 7620作成日:2026年10月23日

Methanol → (2-methylsulfonyl-6-(morpholin-4-yl)-pyrimidin-4-yl]-(5-methyl-2H-pyrazol-3-yl)-amine

https://huagongshe.com/ja/reaction/7620

反応式

関与物質

役割名称HCID仕込み量
反応物MethanolHCID 887—
反応物Potassium hydroxy sulfiteHCID 23707502—
反応物[2-methylsulfanyl-6-(morpholin-4-yl)-pyrimidin-4-yl]-(5-methyl-2H-pyrazol-3-yl)-amineHCID 178419055—
溶媒WaterHCID 962—
生成物(2-methylsulfonyl-6-(morpholin-4-yl)-pyrimidin-4-yl]-(5-methyl-2H-pyrazol-3-yl)-amineHCID 178419103—

反応手順

To a suspension of the above-prepared [2-methylsulfanyl-6-(morpholin-4-yl)-pyrimidin-4-yl]-(5-methyl-2H-pyrazol-3-yl)-amine (500 mg, 1.63 mmol) in MeOH (10 mL) is added a solution of oxone (3.0 g) in water (10 mL). The reaction mixture is stirred at room temperature for 15 hours and most of the solvent is evaporated. The residue is partitioned between DCM and aqueous saturated NaHCO3. The organic layer is washed with brine, dried, filtered and evaporated. The residue is triturated in MeOH and the resulting white solid is collected by filtration to give [2-methylsulfonyl-6-(morpholin-4-yl)-pyrimidin-4-yl]-(5-methyl-2H-pyrazol-3-yl)-amine.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07087603B2
出典データセットuspto-grants-2006_08
ORD IDord-bc09a3a13dce4855b85b4efddef0a94f
出典メモuspto-grants-2006_08