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HRID 58282作成日:2026年10月25日

Ethyl Acetate → 7-(1-aminoethyl)-6-(3-fluorophenyl)-3-methyl-5H-[1,3]thiazolo[3,2-a]pyrimidin-5-one

https://huagongshe.com/reaction/58282

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl AcetateHCID 8857—
反応物TrimethylphosphineHCID 68983—
反応物7-(1-azidoethyl)-6-(3-fluorophenyl)-3-methyl-5H-[1,3]thiazolo[3,2-a]pyrimidin-5-oneHCID 58111402—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
生成物7-(1-aminoethyl)-6-(3-fluorophenyl)-3-methyl-5H-[1,3]thiazolo[3,2-a]pyrimidin-5-oneHCID 5811139998.1%

反応手順

To a stirred solution of 7-(1-azidoethyl)-6-(3-fluorophenyl)-3-methyl-5H-[1,3]thiazolo[3,2-a]pyrimidin-5-one (0.14 g, 0.42 mmol) (1st peak from chiral separation) in tetrahydrofuran (3 mL) and water (0.5 mL) was added 1.00 M of trimethylphosphine in tetrahydrofuran (0.52 mL, 0.52 mmol), and the mixture was stirred at room temperature for 1 hour. To the mixtures were added ethyl acetate and the mixtures were extracted with aqueous 1 N HCl solution (three times). The combined extracts were neutralized with solid NaHCO3, and extracted with dichloromethane (three times). The combined organic layers were washed with brine, dried over MgSO4, and concentrated to give the crude product (0.125 g) used directly in next step. LCMS calculated for C15H15FN3OS (M+H)+: m/z=304.1. Found: 304.0.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09434746B2
出典データセットuspto-grants-2016_09
ORD IDord-c887e060cf974d9988a774b6927d528b
出典メモuspto-grants-2016_09