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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2408779Generated: October 30, 2026

2-Aminobenzenesulfonamide → Ethyl 3-[2-(aminosulfonyl)anilino]-3-oxopropanoate

https://huagongshe.com/reaction/2408779

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminobenzenesulfonamideHCID 72894—
ReactantEthyl 3-chloro-3-oxopropionateHCID 118931—
SolventDiethyl EtherHCID 3283—
SolventDimethylacetamideHCID 31374—
ProductEthyl 3-[2-(aminosulfonyl)anilino]-3-oxopropanoateHCID 14674447—

Reaction Conditions

Temperature25 °C

Reaction Steps

2-Amino-benzenesulfonamide (5 g, 29 mmol) was dissolved in N,N-dimethylacetamide (25 mL) and diethyl ether (25 mL). Ethyl-3-chloro-3-oxo-propionate (4.6 g, 30.45 mmol) was added into the above reaction solution. The reaction mixture was stirred at 25° C. for 3 h. The product started to precipitate and was collected by vacuum filtration. The solid was dissolved in ethyl acetate (200 mL) and extracted with water (200 mL). The aqueous layer was back-extracted with ethyl acetate (200 mL). The combined organic layers were dried over sodium sulfate, filtered, and concentrated in vacuo to afford the crude product, N-(2-sulfamoyl-phenyl)-malonamic acid ethyl ester, as a white solid, which was used in the next step without further purification. 1H NMR (400 MHz, DMSO-d6) δ: 1.23 (3H, t, J=7.0 Hz), 3.61 (2H, s), 4.14 (2H, quartet, J=7.0 Hz), 7.29-7.33 (1H, m), 7.53 (2H, bs), 7.56-7.60 (1H, m), 7.84-7.86 (1H, m), 7.97-7.99 (1H, m), 9.54 (1H, bs). LC-MS (ESI) calcd for C11H14N2O5S 286.06. found 287.1 [M+H+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08815847B2
Source datasetuspto-grants-2014_08
ORD IDord-b3745320d66b4a289e4b6dace4d13894
Source noteuspto-grants-2014_08