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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 252208생성일: 2026년 10월 26일

Triethylamine → Methyl 2-{[(5-methylpyridin-3-yl)amino]sulfonyl}benzoate

https://huagongshe.com/reaction/252208

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Benzoic acid, 2-(chlorosulfonyl)-, methyl esterHCID 117830—
반응물3-Amino-5-methylpyridineHCID 2762894—
용매DichloromethaneHCID 6344—
용매Sodium BicarbonateHCID 516892—
생성물Methyl 2-{[(5-methylpyridin-3-yl)amino]sulfonyl}benzoateHCID 5892407334%

반응 단계

To a solution of 5-methylpyridin-3-amine (0.5 g, 4.62 mmol) in CH2Cl2 (50 ml) were added triethylamine (0.64 mL, 4.62 mmol) and methyl 2-(chlorosulfonyl)benzoate (1.08 g, 4.62 mmol). The resulting mixture was stirred at room temperature for 1 hour. The mixture was then diluted with saturated aqueous NaHCO3 and extracted with CH2Cl2. The organic layer was dried over Na2SO4, filtered and concentrated. The crude residue was purified by flash chromatography (0-8% MeOH/CH2Cl2) to give the title compound (0.476 g, 34%). 1H NMR (400 MHz, DMSO-D6) δ ppm 10.25-10.62 (m, 1H) 8.6 (s, 2H) 7.81-7.93 (m, 1H) 7.64-7.76 (m, 2H) 7.54-7.64 (m, 1H) 7.28 (s, 1H) 3.80 (s, 3H) 2.18 (s, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07868026B2
출처 데이터셋uspto-grants-2011_01
ORD IDord-6f001939915e4bf99a8728db4c5e78d8
출처 메모uspto-grants-2011_01