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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 397054생성일: 2026년 10월 26일

Benzenesulfonyl chloride → 2-Benzenesulfonyl-6-benzyloxy-1-[4-(2-pyrrolidin-1-yl-ethoxy)phenyl]-1,2,3,4-tetrahydroisoquinoline

https://huagongshe.com/reaction/397054

반응식

참여 물질

역할이름HCID투입량
반응물Benzenesulfonyl chlorideHCID 7369—
반응물TriethylamineHCID 8471—
반응물6-Benzyloxy-1-[4-(2-pyrrolidin-1-yl-ethoxy)phenyl]-1,2,3,4-tetrahydroisoquinolineHCID 18172417—
용매TetrahydrofuranHCID 8028—
생성물2-Benzenesulfonyl-6-benzyloxy-1-[4-(2-pyrrolidin-1-yl-ethoxy)phenyl]-1,2,3,4-tetrahydroisoquinolineHCID 17814121168%

반응 단계

Benzenesulfonyl chloride (0.016 g, 0.09 mmol) was added to a solution of 6-benzyloxy-1-[4-(2-pyrrolidin-1-yl-ethoxy)phenyl]-1,2,3,4-tetrahydroisoquinoline (0.040 g, 0.09 mmol) and Et3N (0.026 ml, 0.19 mmol) in anhydrous THF (10 ml) at rt under N2. The resulting suspension was stirred at rt for 18 hr, then evaporated in vacuo to give 0.086 g of yellow residue. Purification by flash chromatography, eluting with EtOAc:MeOH (6:4) gave 0.045 g (85% yield) of white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06608203B2
출처 데이터셋uspto-grants-2003_08
ORD IDord-662bba32657f436f9e8a2e32302e38b7
출처 메모uspto-grants-2003_08