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HRID 2079790作成日:2026年10月27日

Water → 2-(6-{(Naphthalene-2-sulfonyl)-[2-(2-oxopyrrolidin-1-yl)ethyl]amino}-3-azabicyclo[3.1.0]hex-3-yl)pyrimidine-5-carboxylic acid

https://huagongshe.com/reaction/2079790

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Hydroxyamine hydrochlorideHCID 443297—
反応物Sodium ethoxideHCID 2723922—
反応物Ethyl 2-(6-{(naphthalene-2-sulfonyl)-[2-(2-oxopyrrolidin-1-yl)ethyl]amino}-3-azabicyclo[3.1.0]hex-3-yl)pyrimidine-5-carboxylateHCID 59367586—
溶媒EthanolHCID 702—
生成物2-(6-{(Naphthalene-2-sulfonyl)-[2-(2-oxopyrrolidin-1-yl)ethyl]amino}-3-azabicyclo[3.1.0]hex-3-yl)pyrimidine-5-carboxylic acidHCID 5936763532%

反応条件

温度40 °C

反応手順

To a solution of ethyl 2-(6-{(naphthalene-2-sulfonyl)-[2-(2-oxopyrrolidin-1-yl)ethyl]amino}-3-azabicyclo[3.1.0]hex-3-yl)pyrimidine-5-carboxylate (0.749 g, 1.4 mmol) in EtOH (8 ml) was added sodium ethoxide (1.08 g, 15.8 mmol) and hydroxylamine hydrochloride (1.30 g, 18.7 mmol). The mixture was stirred at 40° C. for 18 h, then water (20 ml) was added. The product was extracted with DCM (2×100 ml), and the combined organic extracts were dried (MgSO4) and concentrated in vacuo. The expected hydroxamate product was in fact proved not to have formed. The reaction yielded instead the acid. Purification by reverse phase HPLC yielded the title compound (232 mg, 32%). This was used directly in the next step without characterisation.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07932246B2
出典データセットuspto-grants-2011_04
ORD IDord-4c5f0e421843415b8249f550bea273fc
出典メモuspto-grants-2011_04