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HRID 466362作成日:2026年10月26日

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

https://huagongshe.com/reaction/466362

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物DichloromethaneHCID 6344—
反応物(Dimethyl sulfide)trihydroboronHCID 12423031—
反応物N-Ethyl-n-heptyl-4-(4-(methylsulfonamido)phenyl)-4-oxobutanamideHCID 14891420—
反応物N-(4-Acetyl-2-methylphenyl)methanesulfonamideHCID 19873430—
溶媒EthanolHCID 702—
溶媒MethanolHCID 887—
溶媒TetrahydrofuranHCID 8028—
生成物N-(4-(4-(Ethylheptylamino)butyl)phenyl)methanesulfonamideHCID 9864094—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05155268
出典データセットuspto-grants-1992_10
ORD IDord-2995cb731ad84016ba70e90dafb70e97
出典メモuspto-grants-1992_10