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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2300976Generated: October 29, 2026

Triethylamine → N-tert.-butyl-2-dimethylaminocarbonyl-5-propionylamino-benzenesulfonamide

https://huagongshe.com/reaction/2300976

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantPropionyl chlorideHCID 62324—
Reactant5-Amino-n-tert.-butyl-2-dimethylaminocarbonylbenzenesulfonamideHCID 15240544—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductN-tert.-butyl-2-dimethylaminocarbonyl-5-propionylamino-benzenesulfonamideHCID 15240547—

Reaction Conditions

Temperature5 °C

Reaction Steps

0.85 g of 5-amino-N-tert.-butyl-2-dimethylaminocarbonyl-benzenesulfonamide (Example e) is dissolved in 3.5 ml of DMF at 0° C., and 0.28 g of propionyl chloride and 0.50 ml of triethylamine are added. After the mixture has been stirred at 5° C. for 1 hour, it is taken up in ethyl acetate and washed successively with dilute hydrochloric acid and water. After the mixture has been dried over MgSO4 and the organic phase has been concentrated, 0.60 g of a highly viscous substance, which is employed in subsequent reactions without further purification (Example k), is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06498253B1
Source datasetuspto-grants-2002_12
ORD IDord-f2fe4e34ef194121a07c4ce8d286d137
Source noteuspto-grants-2002_12