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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1925727생성일: 2026년 10월 27일

4-t-Butylbenzenesulfonyl chloride → Methyl 3-(4-tert-butylphenylsulfonamido)thieno[2,3-b]pyridine-2-carboxylate

https://huagongshe.com/reaction/1925727

반응식

참여 물질

역할이름HCID투입량
반응물4-t-Butylbenzenesulfonyl chlorideHCID 139882—
반응물Ethyl 3-aminothieno[2,3-b]pyridine-2-carboxylateHCID 738459—
용매WaterHCID 962—
용매PyridineHCID 1049—
생성물Methyl 3-(4-tert-butylphenylsulfonamido)thieno[2,3-b]pyridine-2-carboxylateHCID 5918044012.8%

반응 단계

To a solution of ethyl 3-aminothieno[2,3-b]pyridine-2-carboxylate (0.3 g; 1.35 mmol) in pyridine (10 mL) was added 4-tert-butylbenzenesulfonyl chloride (0.48 g; 2.03 mol). The reaction was stirred at room temperature for 18 hours and then diluted with water and extracted with ethyl acetate. The organic layer was separated and successively washed with aqueous hydrochloric acid (2N) and aqueous saturated sodium chloride solution, dried over magnesium sulfate, filtered, and evaporated under reduced pressure. The crude residue was purified by silica gel chromatography eluting with hexanes/ethyl acetate to yield the title compound as a white solid (0.070 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08178699B2
출처 데이터셋uspto-grants-2012_05
ORD IDord-a4869878b4d840e09171b5f06e6b4f2c
출처 메모uspto-grants-2012_05