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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 713665생성일: 2026년 10월 27일

Sodium Bicarbonate → 3-ethylsulfanyl-N-[4-(2,2,2-trifluoro-1,1-dimethoxyethyl)phenyl]picolinamide

https://huagongshe.com/reaction/713665

반응식

참여 물질

역할이름HCID투입량
반응물Sodium BicarbonateHCID 516892—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
반응물3-(Ethylsulfanyl)pyridine-2-carboxylic acidHCID 79006954—
반응물4-(2,2,2-Trifluoro-1,1-dimethoxyethyl)anilineHCID 118113465—
촉매1-HydroxybenzotriazoleHCID 75771—
용매PyridineHCID 1049—
생성물3-ethylsulfanyl-N-[4-(2,2,2-trifluoro-1,1-dimethoxyethyl)phenyl]picolinamideHCID 11811341389.4%

반응 단계

A mixture of 0.38 g of 4-(2,2,2-trifluoro-1,1-dimethoxyethyl)aniline, 0.22 g of 3-ethylsulfanylpicolinic acid, 0.29 g of EDCI hydrochloride, 0.01 g of HOBt and 5 mL of pyridine was stirred at room temperature for 2 hours. A saturated aqueous sodium bicarbonate solution was poured to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was dried over anhydrous sodium sulfate and then concentrated under reduced pressure, and the resulting residue was applied to a silica gel column chromatography to obtain 0.43 g of 3-ethylsulfanyl-N-[4-(2,2,2-trifluoro-1,1-dimethoxyethyl)phenyl]picolinamide (Compound of Present Invention 58).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09185910B2
출처 데이터셋uspto-grants-2015_11
ORD IDord-acc110fd4c104b7da7e5a3017d460713
출처 메모uspto-grants-2015_11