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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 527363Generated: November 2, 2026

Dimethylamine → 4-((1,3-Dioxoisoindolin-2-yl)methyl)-N,N,N'-trimethyl-benzene-sulfonimidamide

https://huagongshe.com/reaction/527363

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylamineHCID 674—
ReactantWaterHCID 962—
ReactantTert-Butyl hypochloriteHCID 521297—
Reactant4-(1,3-Dioxo-1,3-dihydro-isoindol-2-ylmethyl)-benzenesulfinic acid methylamideHCID 86711634—
SolventAcetonitrileHCID 6342—
Product4-((1,3-Dioxoisoindolin-2-yl)methyl)-N,N,N'-trimethyl-benzene-sulfonimidamideHCID 89978766—

Reaction Conditions

Temperature0 °C

Reaction Steps

A mixture of 4-(1,3-dioxo-1,3-dihydro-isoindol-2-ylmethyl)-benzenesulfinic acid methylamide (preparation 60b, 250 mg, 0.795 mmol) in acetonitrile is cooled at 0° C. in an ice bath and treated with tert-butyl hypochlorite (100 μL, 0.88 mmol). After 15 min dimethylamine (2 M in tetrahydrofuran, 600 μL, 1.2 mmol) is added and the mixture is warmed to room temperature. Water is added, and the mixture is extracted twice with dichloromethane. The combined organic layers are dried over Na2SO4 and concentrated under reduced pressure. The residue is purified by flash chromatography on silica (gradient cyclohexane/ethyl acetate 7:3 to ethyl acetate). Yield: 284 mg (99% of theory). ESI mass spectrum: [M+H]+=358; r.t. HPLC: 0.43 min (X012_S01).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09346794B1
Source datasetuspto-grants-2016_05
ORD IDord-f5e32827a84b4964a93a10e82a927088
Source noteuspto-grants-2016_05