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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 84967생성일: 2026년 10월 24일

Benzenesulfonyl chloride, 3,4-dichloro- → tert-Butyl trans-6-[(3,4-dichlorophenyl)sulfonyl]-6,7,7a,8,10,10a-hexahydropyrido[3,2-c]pyrrolo[3,4-e]azepine-9(5H)-carboxylate

https://huagongshe.com/ko/reaction/84967

반응식

참여 물질

역할이름HCID투입량
반응물Benzenesulfonyl chloride, 3,4-dichloro-HCID 7383—
반응물TriethylamineHCID 8471—
반응물Sodium HydroxideHCID 14798—
반응물tert-Butyl trans-6,7,7a,8,10,10a-hexahydropyrido[3,2-c]pyrrolo[3,4-e]azepine-9(5H)-carboxylateHCID 123947677—
용매DichloromethaneHCID 6344—
생성물tert-Butyl trans-6-[(3,4-dichlorophenyl)sulfonyl]-6,7,7a,8,10,10a-hexahydropyrido[3,2-c]pyrrolo[3,4-e]azepine-9(5H)-carboxylateHCID 123445055—

반응 단계

A mixture of Example 334B (100 mg, 0.34 mmol) and triethylamine (0.097 mL, 0.69 mmol) in dichloromethane (2 mL) was stirred at ambient temperature for 10 minutes. 3,4-Dichlorobenzene-1-sulfonyl chloride (0.52 mmol, 1.5 equivalents) was added, and the reaction mixture was stirred at room temperature overnight. A 10% NaOH solution (2 mL) was added; the dichloromethane layer was separated, treated with water (2 mL) and dried over Na2SO4. The solvent was removed in vacuo to give the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08846951B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-f6e17a941eae4d229020d7b4426a778f
출처 메모uspto-grants-2014_09