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HRID 215840作成日:2026年10月23日

Triphenylphosphine → (1S,4R)-4-(2,6-Dichloro-9H-purin-9-yl)cyclopent-2-en-1-ol

https://huagongshe.com/ja/reaction/215840

反応式

関与物質

役割名称HCID仕込み量
反応物TriphenylphosphineHCID 11776—
反応物2,6-DichloropurineHCID 5324412—
反応物rac-(1R,4S)-4-hydroxycyclopent-2-en-1-yl acetateHCID 10154103—
触媒Bis(dibenzylideneacetone)palladiumHCID 9811564—
生成物(1S,4R)-4-(2,6-Dichloro-9H-purin-9-yl)cyclopent-2-en-1-olHCID 10378467—

反応手順

2,6-Dichloropurine (10 g, 52.90 mmol), (1S,4R)-cis 4-acetoxy-2-cyclopenten-1-ol (10 g, 70.40 mmol), tris(dibenzylideneacetone)dipalladium(0) (3.20 g, 3.50 mmol) and polymer supported triphenylphosphine (3 mmol/g, 11.60 g, 35.00 mmol) are placed in an oven-dried flask under an atmosphere of argon. Dry deoxygenated THF (80 mL) is added and the reaction mixture is stirred gently for 5 minutes. TEA (20 mL) is added and the reaction mixture is stirred at 50° C. The reaction is shown to be complete by LCMS after 1 hour. The reaction mixture is allowed to cool, filtered and the solvent is removed in vacuo. The title compound is obtained after purification by flash column chromatography (silica, DCM:MeOH 25:1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08193164B2
出典データセットuspto-grants-2012_06
ORD IDord-4f16a5b7b5164838bfb0298f2cd8ca8a
出典メモuspto-grants-2012_06