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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1827549생성일: 2026년 10월 25일

Triethylamine → 2-Cyano-N-[4-(2-pyrrolidin-1-yl-ethoxy)-phenyl]-N-[3-(tetrahydro-pyran-2-yloxy)-benzyl]-benzenesulfonamide

https://huagongshe.com/reaction/1827549

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Sodium BicarbonateHCID 516892—
반응물2-Cyanobenzenesulfonyl ChlorideHCID 522347—
반응물HCID 22137433HCID 22137433—
용매DichloromethaneHCID 6344—
생성물2-Cyano-N-[4-(2-pyrrolidin-1-yl-ethoxy)-phenyl]-N-[3-(tetrahydro-pyran-2-yloxy)-benzyl]-benzenesulfonamideHCID 22137283—

반응 단계

To a solution of [4-(2-pyrrolidin-1-yl-ethoxy)-phenyl]-[3-(tetrahydro-pyran-2-yloxy)-benzyl]-amine (0.091 g, 0.23 mmol) and triethylamine (0.097 mL, 0.69 mmol) in 2 mL methylene chloride was added 2-cyanobenzenesulfonyl chloride (0.093 g, 0.46 mmol). The reaction mixture was stirred at room temperature for 24 hr. Saturated aqueous sodium bicarbonate was added and the layers were separated. The aqueous layer was washed with an additional 2 mL of methylene chloride. The combined organic layers were concentrated to afford the title compound of Step A.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07053212B2
출처 데이터셋uspto-grants-2006_05
ORD IDord-b687e3e9f1574b49a08d89f017c2da74
출처 메모uspto-grants-2006_05