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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1697270Generated: October 26, 2026

Benzylamine → 6-(3,5-Dichloro-phenylsulphonylamino)-naphthalene-1-carboxylic acid-benzylamide

https://huagongshe.com/reaction/1697270

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzylamineHCID 7504—
ReactantDiisopropylethylamineHCID 81531—
ReactantO-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
Reactant6-(3,5-Dichloro-phenylsulphonylamino)-naphthalene-1-carboxylic acidHCID 58496966—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product6-(3,5-Dichloro-phenylsulphonylamino)-naphthalene-1-carboxylic acid-benzylamideHCID 59534111—

Reaction Steps

1.50 ml diisopropylethylamine and 2.81 g O-(benzotriazol-1-yl)-1,1,3,3-tetramethyluronium-tetrafluoroborate are added to 3.47 g 6-(3,5-dichloro-phenylsulphonylamino)-naphthalene-1-carboxylic acid in 15 ml N,N-dimethylformamide. The reaction mixture is stirred for 15 minutes at ambient temperature, then 0.97 ml benzylamine and 1.50 ml diisopropylethylamine are added and the mixture is stirred for a further two hours at ambient temperature. For working up the reaction mixture is mixed with water and extracted with ethyl acetate. The combined organic extracts are washed with 1N hydrochloric acid, 1N sodium hydroxide solution and saturated sodium chloride solution, dried on magnesium sulphate and evaporated down. The foam-like flask residue is stirred overnight with cyclohexane/ethyl acetate and the resulting crystalline precipitate is suction filtered, washed with cyclohexane and dried.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08163911B2
Source datasetuspto-grants-2012_04
ORD IDord-544393e52cff49298097fa50c485f823
Source noteuspto-grants-2012_04