HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 884248Generated: October 26, 2026
2-Aminobenzenesulfonamide → Ethyl 3-[2-(aminosulfonyl)anilino]-3-oxopropanoate
https://huagongshe.com/reaction/884248
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Aminobenzenesulfonamide | HCID 72894 | — |
| Reactant | Ethyl 3-chloro-3-oxopropionate | HCID 118931 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | Ethyl 3-[2-(aminosulfonyl)anilino]-3-oxopropanoate | HCID 14674447 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08236948B2 |
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| Source dataset | uspto-grants-2012_08 |
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| ORD ID | ord-272396264f3249a88fcbfa96aa42b373 |
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| Source note | uspto-grants-2012_08 |
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