HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1461032Generated: October 27, 2026
HCID 178471895, compound → ethyl 2-[2-amino-5-(difluoromethoxy)-3,4,6-trifluorobenzoyl]-3-(cyclopropylamino)prop-2-enoate
https://huagongshe.com/reaction/1461032
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 178471895 | HCID 178471895 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | ethyl 2-[2-amino-5-(difluoromethoxy)-3,4,6-trifluorobenzoyl]-3-(cyclopropylamino)prop-2-enoate | HCID 178471897 | 80.6% |
Reaction Steps
33.63 g (0.079 mole) of ethyl 3-cyclopropylamino-2-(3-difluoromethoxy-2,4,5-trifluoro-6-nitrobenzoyl)acrylate [(XIXa): X=X'=F, R1 =OCHF2, R17 =C2H5 ] were dissolved in 1300 ml of ethanol with heating. A stream of hydrogen was then bubbled through the solution in the presence of 8.4 g of 5% w/w palladium-on-carbon at room temperature for 40 minutes, whilst stirring. At the end of this time, the reaction mixture was filtered, and the filtrate was concentrated by evaporation under reduced pressure. The resulting residue was then purified by silica gel column chromatography using a 9:1 by volume mixture of toluene and ethyl acetate as the eluent, to give 25.1 g of ethyl 3-cyclopropylamino-2-(6-amino-3-difluoromethoxy-2,4,5-trifluorobenzoyl)acrylate [(XIXb): X=X'=F, R1 =OCHF2, R17 =C2H5 ] as a pale yellow powder, melting at 103°-104° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05073556 |
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| Source dataset | uspto-grants-1991_12 |
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| ORD ID | ord-cde91cd436284f6eb7edf689d4d4bd9e |
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| Source note | uspto-grants-1991_12 |
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