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HRID 1446011作成日:2026年10月27日

3-(Benzylamino)propionitrile → Acetic acid 4-{[benzyl-(2-cyano-ethyl)-amino]-methylene}-6,17-dihydroxy-1-methoxymethyl-10,13-dimethyl-3,7-dioxo-1,3,4,7,10,11,12,13,14,15,16,17-dodecahydro-2-oxa-cyclopenta[a]phenanthren-11-yl ester

https://huagongshe.com/reaction/1446011

反応式

関与物質

役割名称HCID仕込み量
反応物3-(Benzylamino)propionitrileHCID 69719—
反応物17beta-Hydroxy wortmanninHCID 9867340—
溶媒DichloromethaneHCID 6344—
生成物Acetic acid 4-{[benzyl-(2-cyano-ethyl)-amino]-methylene}-6,17-dihydroxy-1-methoxymethyl-10,13-dimethyl-3,7-dioxo-1,3,4,7,10,11,12,13,14,15,16,17-dodecahydro-2-oxa-cyclopenta[a]phenanthren-11-yl esterHCID 68541487—

反応手順

To a solution of 100 mg (0.23 mmol) 17-hydroxywortmannin in 2 mL CH2Cl2 is added 3-benzylamino-propionitrile (73 μL, 0.46 mmol). The reaction mixture is stirred at room temperature for 12 hours and then concentrated in vacuo. The residue is dissolved in EtOAc and precipitated with hexane. The precipitate is washed two times with hexane to give the product as a yellow solid. MS (ESI) m/z 592 (M+H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07666901B2
出典データセットuspto-grants-2010_02
ORD IDord-9fca3092b9324c28923b67d68dcdfe10
出典メモuspto-grants-2010_02