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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1099658생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1099658

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물5-Bromonicotinic acidHCID 88707—
반응물Benzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphateHCID 151348—
반응물ethyl(S-phenylsulfonimidoyl)acetateHCID 76585231—
용매DimethylformamideHCID 6228—
생성물(S)-Ethyl {N-[(5-bromopyridin-3-yl)carbonyl]-S-phenylsulfonimidoyl}acetateHCID 5765789034%

반응 단계

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%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08143410B2
출처 데이터셋uspto-grants-2012_03
ORD IDord-bed780b4759d4b788659997d4e99fab6
출처 메모uspto-grants-2012_03