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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2079790생성일: 2026년 10월 27일

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

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참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Hydroxyamine hydrochlorideHCID 443297—
반응물Sodium ethoxideHCID 2723922—
반응물Ethyl 2-(6-{(naphthalene-2-sulfonyl)-[2-(2-oxopyrrolidin-1-yl)ethyl]amino}-3-azabicyclo[3.1.0]hex-3-yl)pyrimidine-5-carboxylateHCID 59367586—
용매EthanolHCID 702—
생성물2-(6-{(Naphthalene-2-sulfonyl)-[2-(2-oxopyrrolidin-1-yl)ethyl]amino}-3-azabicyclo[3.1.0]hex-3-yl)pyrimidine-5-carboxylic acidHCID 5936763532%

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온도40 °C

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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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07932246B2
출처 데이터셋uspto-grants-2011_04
ORD IDord-4c5f0e421843415b8249f550bea273fc
출처 메모uspto-grants-2011_04