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HRID 2194208作成日:2026年10月27日

(Diethylamino)sulfur trifluoride → 8-(2-Chloro-benzenesulfonyl)-2-[4-(3-fluoro-oxetan-3-yl)-phenyl]-2,8-diaza-spiro[4.5]decan-1-one

https://huagongshe.com/reaction/2194208

反応式

関与物質

役割名称HCID仕込み量
反応物(Diethylamino)sulfur trifluorideHCID 123472—
反応物8-(2-Chloro-benzenesulfonyl)-2-[4-(3-hydroxy-oxetan-3-yl)-phenyl]-2,8-diaza-spiro[4.5]decan-1-oneHCID 59577907—
溶媒DichloromethaneHCID 6344—
生成物8-(2-Chloro-benzenesulfonyl)-2-[4-(3-fluoro-oxetan-3-yl)-phenyl]-2,8-diaza-spiro[4.5]decan-1-oneHCID 5957806641.8%

反応条件

温度-78 °C

反応手順

To a solution of 8-(2-chloro-benzenesulfonyl)-2-[4-(3-hydroxy-oxetan-3-yl)-phenyl]-2,8-diaza-spiro[4.5]decan-1-one (described in example 229, 35 mg, 0.07 mmol) in DCM was added DAST (11 uL, 0.08 mmol) at −78° C. The reaction mixture was stirred at −78° C. for 3 hr and then quenched with sat. NaHCO3. The reaction mixture was diluted with DCM and washed with brine, dried (Na2SO4), filtered and concentrated in vacuo to give a crude residue which was purified by flash column chromatography (1:1 AcOEt/heptane) to give 8-(2-chloro-benzenesulfonyl)-2-[4-(3-fluoro-oxetan-3-yl)-phenyl]-2,8-diaza-spiro[4.5]decan-1-one (14 mg, 40%) as a white solid. MS (ESI): 479.1 (MH+).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08329904B2
出典データセットuspto-grants-2012_12
ORD IDord-b72f92127bc846ceb01632654226e47a
出典メモuspto-grants-2012_12