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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1479412생성일: 2026년 10월 25일

Ethylenediamine → N-(2-aminoethyl)-3-(6,8-dichloro-2-methyl-1,2,3,4-tetrahydroisoquinolin-4-yl)benzenesulfonamide

https://huagongshe.com/reaction/1479412

반응식

참여 물질

역할이름HCID투입량
반응물EthylenediamineHCID 3301—
반응물3-(6,8-Dichloro-2-methyl-1,2,3,4-tetrahydroisoquinolin-4-yl)benzene-1-sulfonyl chlorideHCID 86672330—
용매DichloromethaneHCID 6344—
용매dichloromethane N,N-dimethylformamideHCID 22350042—
생성물N-(2-aminoethyl)-3-(6,8-dichloro-2-methyl-1,2,3,4-tetrahydroisoquinolin-4-yl)benzenesulfonamideHCID 6745725383.5%

반응 단계

Into a 50-mL 3-necked round-bottom flask purged and maintained with an inert atmosphere of nitrogen, was placed a solution of 3-(6,8-dichloro-2-methyl-1,2,3,4-tetrahydroisoquinolin-4-yl)benzene-1-sulfonyl chloride (intermediate 1.6) (100 mg, 0.26 mmol, 1.00 equiv) in DCM (5 mL). This was followed by the addition of a solution of ethane-1,2-diamine (307 mg, 5.11 mmol, 19.96 equiv) in DCM/DMF (10/1 mL). The resulting solution was stirred for 5 h at room temperature. The mixture was concentrated under vacuum. The resulting solution was diluted with 50 mL of ethyl acetate and washed with 2×10 mL of water and then 1×10 mL of Brine. The organic layer was dried over anhydrous sodium sulfate and concentrated under vacuum to afford 90 mg (76%) of N-(2-aminoethyl)-3-(6,8-dichloro-2-methyl-1,2,3,4-tetrahydroisoquinolin-4-yl)benzenesulfonamide as yellow oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09408840B2
출처 데이터셋uspto-grants-2016_08
ORD IDord-d5665fda28f74513aee1e735a19f278b
출처 메모uspto-grants-2016_08