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HRID 395888作成日:2026年10月26日

8-Oxabicyclo[3.2.1]oct-6-en-3-one → HCID 178456493、化合物

https://huagongshe.com/reaction/395888

反応式

関与物質

役割名称HCID仕込み量
反応物8-Oxabicyclo[3.2.1]oct-6-en-3-oneHCID 557672—
反応物8-(8-Hydroxy-8-methyl-bicyclo[3.2.1]oct-3-yl)-1,3-dipropyl-3,7-dihydro-purine-2,6-dioneHCID 18173101—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
生成物HCID 178456493HCID 178456493—

反応手順

To a stirred solution of 1,3-dipropyl-7-pyrrolidin-1-ylmethyl-3,7-dihydro-purine-2,6-dione (Example 48) (522 mg, 1.63 mmol) in THF (50 ml) at −78° C. was added n-BuLi (1.55 M in hexanes, 1.2 eq, 1.3 ml). The color of the resulting yellow mixture deepened to orange-red and was stirred at this temperature for 0.5 h. A solution of 8-oxa-bicyclo[3.2.1]oct-6-en-3-one (1.1 eq, 222 mg, 1.79 mmol) in THF (4 ml) was added via syringe over a period of 20 minutes. The mixture was held at −78° C. for 2 h and allowed to reach ambient temperature overnight (12 h). The reaction mixture was partitioned between saturated aqeuous NH4Cl (20 ml) and EtOAc (20 ml) and the aqueous phase was extracted with EtOAc (20 ml). The combined organic extracts were washed with saturated aqeuous NaCl (20 ml), dried (MgSO4), filtered and concentrated in vacuo. The resulting orange oil was purified by chromatography on silica using 5% MeOH in CH2Cl2 as eluent to give a clear oil that solidified upon standing (50 mg, 8%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06605600B1
出典データセットuspto-grants-2003_08
ORD IDord-2f7ed1c428dc4bc2831aeccb59e669aa
出典メモuspto-grants-2003_08