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HRID 61489作成日:2026年10月24日

Sodium bis(trimethylsilyl)amide → Methyl (1s,2s,5e)-5-benzylidene-2-[(4-phenylpiperazin-1-yl)carbonyl]cyclohexanecarboxylate

https://huagongshe.com/ja/reaction/61489

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium bis(trimethylsilyl)amideHCID 2724254—
反応物Benzyltriphenylphosphonium bromideHCID 2734970—
反応物Methyl (1s,2s)-5-oxo-2-[(4-phenylpiperazin-1-yl)carbonyl]cyclohexanecarboxylateHCID 67304345—
溶媒TetrahydrofuranHCID 8028—
生成物Methyl (1s,2s,5e)-5-benzylidene-2-[(4-phenylpiperazin-1-yl)carbonyl]cyclohexanecarboxylateHCID 67304520—

反応手順

To a suspension of benzyltriphenylphosphonium bromide (0.397 g, 0.000880 mol) in anhydrous THF (3.0 mL) at rt was added 1.00 M of sodium bis(trimethylsilyl)amide in tetrahydrofuran (0.880 mL) dropwise. The resulting orange suspension was stirred at rt for 1 h, a solution of methyl(1S,2S)-5-oxo-2-[(4-phenylpiperazin-1-yl)carbonyl]cyclohexanecarboxylate (202 mg, 0.000586 mol) in anhydrous THF (3.0 mL) was then added via cannula. The reaction mixture was stirred at rt for 18 h. The reaction was quenched with water (20 mL), extracted with EtOAc (2×). The combined organic layers were washed with brine, dried over sodium sulfate, filtered and concentrated in vacuo. The residue was purified by Combiflash with 20-60% EtOAc/Hex to give the product (141 mg, 57% in yield) as well as the S.M. (50 mg, 25% recovery of S.M.). MS (ESI): (M+H)+=419.2.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09440958B2
出典データセットuspto-grants-2016_09
ORD IDord-b70ab8e192c445b3968a739d462c372e
出典メモuspto-grants-2016_09