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HRID 888295作成日:2026年10月27日

Water → 8-(4-(4-Methoxyphenyl)-5-(p-tolyl)thiazol-2-yl)-1,4-dioxaspiro[4.5]decan-8-ol

https://huagongshe.com/reaction/888295

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物2-(Benzenesulfonyl)-3-phenyloxaziridineHCID 320405—
反応物8-(4-(4-Methoxyphenyl)-5-(p-tolyl)thiazol-2-yl)-1,4-dioxaspiro[4.5]decaneHCID 67296392—
溶媒TetrahydrofuranHCID 8028—
溶媒HexaneHCID 8058—
溶媒ButyllithiumHCID 178418339—
生成物8-(4-(4-Methoxyphenyl)-5-(p-tolyl)thiazol-2-yl)-1,4-dioxaspiro[4.5]decan-8-olHCID 6729642455%

反応手順

To a solution of 8-(4-(4-methoxyphenyl)-5-(p-tolyl)thiazol-2-yl)-1,4-dioxaspiro[4.5]decane (Reference Example 95) (734 mg, 1.74 mmol) in tetrahydrofuran (8.7 mL), 1.63 M n-butyllithium/solution in n-hexane (1.17 mL) was added at −78° C., and the obtained solution was stirred at the same temperature for 1 hour. The reaction solution was added at −78° C. to a solution of 3-phenyl-2-(phenylsulfonyl)-1,2-oxaziridine (546 mg, 2.09 mmol) in tetrahydrofuran (8.7 mL), and the obtained solution was allowed to warm gradually to room temperature with stirring. Distilled water was added to the reaction solution, and the resulting solution was extracted with ethyl acetate. The organic layer was washed with brine, dried over sodium sulfate and concentrated under reduced pressure. The residue was purified by flash chromatography (silica gel, n-hexane/ethyl acetate) to obtain the captioned compound (417 mg, 0.954 mmol, 55%) as a colorless amorphous product.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08247569B2
出典データセットuspto-grants-2012_08
ORD IDord-5d01bba6dc0f4998b5d7ce065be207e8
出典メモuspto-grants-2012_08