戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1099658作成日:2026年10月26日

Diisopropylethylamine → (S)-Ethyl {N-[(5-bromopyridin-3-yl)carbonyl]-S-phenylsulfonimidoyl}acetate

https://huagongshe.com/reaction/1099658

反応式

関与物質

役割名称HCID仕込み量
反応物DiisopropylethylamineHCID 81531—
反応物5-Bromonicotinic acidHCID 88707—
反応物Benzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphateHCID 151348—
反応物ethyl(S-phenylsulfonimidoyl)acetateHCID 76585231—
溶媒DimethylformamideHCID 6228—
生成物(S)-Ethyl {N-[(5-bromopyridin-3-yl)carbonyl]-S-phenylsulfonimidoyl}acetateHCID 5765789034%

反応手順

To a solution of 5-bromonicotinic acid (343 mg, 1.66 mmol) in anhydrous DMF (5.5 μL) was added N,N-diisopropylethylamine (0.58 mL, 3.32 mmol) and ethyl (S-phenylsulfonimidoyl)acetate (415 mg, 1.83 mmol) followed by the final addition of (benzotriazol-1-yloxy)-tris(dimethylamino)-phosphonium hexafluorophophate (0.81 g, 1.83 mmol). The reaction mixture was stirred at room temperature for 20 min, and then partitioned between saturated aqueous NaHCO3 and EtOAc. The organic layer was separated and washed once with brine and dried over anhydrous Na2SO4. The organic layer was concentrated and the residue purified by chromatography (silica gel, gradient elution (5:1 Hexane/EtOAc to 3:1 Hexane/EtOAc). The product containing fractions were concentrated to give the title compound as a white solid (230 mg, 34%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08143410B2
出典データセットuspto-grants-2012_03
ORD IDord-bed780b4759d4b788659997d4e99fab6
出典メモuspto-grants-2012_03