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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 530343생성일: 2026년 10월 25일

Triethylamine → N-(4-Bromo-5,6,7,8-tetrahydro-8-isoquinolinyl)ethanesulfonamide

https://huagongshe.com/reaction/530343

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Ethanesulfonyl chlorideHCID 11667—
반응물4-Bromo-5,6,7,8-tetrahydroisoquinolin-8-amineHCID 71743379—
용매DichloromethaneHCID 6344—
생성물N-(4-Bromo-5,6,7,8-tetrahydro-8-isoquinolinyl)ethanesulfonamideHCID 8945848195%

반응 단계

To a solution of (rac)-4-bromo-5,6,7,8-tetrahydro-isoquinolin-8-ylamine (intermediate A-2 [D]) (227 mg, 1 mmol) and Et3N (152 mg, 1.5 mmol) in DCM (5 mL) was added ethanesulfonyl chloride (193 mg, 1.5 mmol) at 0° C. The reaction mixture was stirred at room temperature for 1 hr before it was concentrated in vacuo. The residue was dissolved in ethyl acetate and washed with water and the organic layer was dried over anhy. Na2SO4, filtered, and concentrated in vacuo to give a crude product (302 mg, 95% yield). MS: 319.0 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09353081B2
출처 데이터셋uspto-grants-2016_05
ORD IDord-3934dcafef544f35a44199158b8028b7
출처 메모uspto-grants-2016_05