HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1639304Generated: October 27, 2026
Ammonia → Ethyl N-(2-carbamoyl-5-chlorophenyl)aminoacetate
https://huagongshe.com/reaction/1639304
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 4-Chloroisatoic anhydride | HCID 329105 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Ethyl N-(2-carbamoyl-5-chlorophenyl)aminoacetate | HCID 11780149 | — |
Reaction Steps
To a solution of 7-chloro-2H-3,1-benzoxazine-2,4(1H)-dione (330 g) in N,N-dimethylformamide (3.3 l) was added sodium hydride (60% in mineral oil, 86.8 g) below 20° C. and the mixture was stirred at 5° C. for 30 minutes. To this solution was added ethyl bromoacetate (222 ml) at 10° C. over a 30-minute period and the resulting mixture was stirred at room temperature for 1.5 hours. To this reaction mixture was added 28% aqueous ammonia (696 ml) below 10° C. and the resulting mixture was stirred at 5° C. for 20 minutes. The mixture was poured into 1N hydrochloric acid (16.5 l). The precipitates were collected by filtration, and washed in turn with water (3 times) and diethyl ether to give ethyl N-(2-carbamoyl-5-chlorophenyl)aminoacetate (360 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04883800 |
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| Source dataset | uspto-grants-1989_11 |
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| ORD ID | ord-c8455e6407f94cd08801fdef87410b19 |
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| Source note | uspto-grants-1989_11 |
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