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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 466362생성일: 2026년 10월 24일

Hydrochloric Acid → N-(4-(4-(Ethylheptylamino)butyl)phenyl)methanesulfonamide

https://huagongshe.com/ko/reaction/466362

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물DichloromethaneHCID 6344—
반응물(Dimethyl sulfide)trihydroboronHCID 12423031—
반응물N-Ethyl-n-heptyl-4-(4-(methylsulfonamido)phenyl)-4-oxobutanamideHCID 14891420—
반응물N-(4-Acetyl-2-methylphenyl)methanesulfonamideHCID 19873430—
용매EthanolHCID 702—
용매MethanolHCID 887—
용매TetrahydrofuranHCID 8028—
생성물N-(4-(4-(Ethylheptylamino)butyl)phenyl)methanesulfonamideHCID 9864094—

반응 단계

A stirred solution of N-ethyl-N-heptyl-γ-oxo-4-[(methylsulfonyl)amino]benzenebutanamide as prepared in Preparation 3 (2.0 g, 0.005 mol) in THF (20 ml), under N2, is treated during 1 hour with a 1M solution of borane dimethylsulfide in CH2Cl2 (15.8 ml, 0.0158 mol). The mixture is kept at ambient temperature for 30 minutes and at reflux for 4 hours. It is then cooled in an ice bath and treated slowly with MeOH (2 ml). This mixture is kept at ambient temperature for 18 hours, acidified with a solution of HCl in EtOH and refluxed for 1 hour. The cooled solution is concentrated and the residue is mixed with saturated NaHCO3 and extracted with CH2Cl2. The extracts are washed with brine, dried (Na2SO4) and concentrated. The residue is chromatographed on silica gel (350 g) with 5% MeOH-0.5% NH4OH--CH2Cl2. The N-[4-[4 -(ethylheptylamino)butyl]phenyl]methanesulfonamide thus obtained is mixed with saturated NaHCO3 and extracted with Et2O. The extracts are washed with brine, dried (MgSO4) and concentrated. A solution of the residue in pentane is filtered through Magnisol and concentrated. MS: theory for C20H36N2O2S(M+): 368.2497. Found: 368.2498.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05155268
출처 데이터셋uspto-grants-1992_10
ORD IDord-2995cb731ad84016ba70e90dafb70e97
출처 메모uspto-grants-1992_10