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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 391300생성일: 2026년 10월 25일

5-Bromo-3-pyridinecarboxaldehyde → N-((5-bromopyridin-3-yl)(cyclopropyl)methyl)propane-2-sulfonamide

https://huagongshe.com/reaction/391300

반응식

참여 물질

역할이름HCID투입량
반응물5-Bromo-3-pyridinecarboxaldehydeHCID 2784734—
반응물Propane-2-sulfonamideHCID 3549191—
반응물HCID 178418630HCID 178418630—
촉매Titanium isopropoxideHCID 11026—
용매TolueneHCID 1140—
생성물N-((5-bromopyridin-3-yl)(cyclopropyl)methyl)propane-2-sulfonamideHCID 5957839166%

반응 조건

온도-40 °C

반응 단계

A mixture of 5-bromonicotinaldehyde (0.930 g, 5 mmol), propane-2-sulfonamide (0.616 g, 5.00 mmol) and titanium(IV) isopropoxide (2.93 mL, 10.00 mmol) in toluene (20 mL) was heated to reflux for 4 h. After concentration, the residue was dissolved in THF (25 mL) and cooled to −40° C. A solution of cyclopropylmagnesium bromide (25 mL, 12.50 mmol) was added dropwise and the resulting mixture was slowly warmed up to 0° C. over 4 h. After quenching with a NH4Cl solution, filtration and extraction with CH2Cl2, the organic phase was dried over Na2SO4, filtered and concentrated, to give a residue which was purified by flash column (ethyl acetate/heptane, v/v, 10%-35%) and to give a yellow solid (1.1 g). ESI-MS m/z: 335.0 [M+1]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08383827B2
출처 데이터셋uspto-grants-2013_02
ORD IDord-8e4e0f0205eb4c91aa016ffcf0ac200e
출처 메모uspto-grants-2013_02