HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 448821Generated: October 29, 2026
Water → Methyl 4-(4-chloro-2-(1-cyclopropylethylcarbamoyl)phenylamino)-4-oxocrotonate
https://huagongshe.com/reaction/448821
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | methyl (E)-3-(6-chloro-4-oxo-4H-benzo[d][1,3]oxazin-2-yl)acrylate | HCID 13927266 | — |
| Reactant | 1-Cyclopropylethylamine hydrochloride | HCID 16247869 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Methyl 4-(4-chloro-2-(1-cyclopropylethylcarbamoyl)phenylamino)-4-oxocrotonate | HCID 44185603 | — |
Reaction Steps
A mixed solution of 0.73 g of 1-cyclopropylethylamine hydrochloride and 0.91 g of triethylamine in 12 ml of acetonitrile was stirred at room temperature for one hour. Then, to the mixed solution, 0.53 g of crude crystals of methyl (E)-3-(6-chloro-4-oxo-4H-benzo[d][1,3]oxazin-2-yl)acrylate were added at room temperature and reacted for 3 hours at room temperature. To the reaction liquid, water was added, and then ethyl acetate was added for extraction. The organic layer was washed with a saturated sodium chloride aqueous solution and dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressed, and the residue was purified by silica gel column chromatography (eluent: n-hexane/ethyl acetate=9/1 to 8/2) to obtain 0.22 g of the desired product having a slightly yellow color (melting point: 154.4° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08481744B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-b0436f365e064f189be42a580ea0c529 |
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| Source note | uspto-grants-2013_07 |
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