Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | 3-Ethoxy-4-hydroxy-5-nitrobenzaldehyde | HCID 584878 | — |
| Reactant | 2-cyano-N,N-bis(ethylamino)acetamide | HCID 86611404 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Entacapone Impurity 55 | HCID 69218750 | 172.7% |
Reaction Steps
A flask was charged with 3-ethoxy-4-hydroxy-5-nitrobenzaldehyde (20 g, 0.0947 mole) (formula 2 where R is ethyl) and N,N-diethylaminocyanoacetamide (formula (3)) (14.6 g, 0.1042 mol), acetic acid (3.13 g), and piperidine (4.45 g), along with toluene (200 mL), and was heated to a reflux temperature of about 100-115° C. with continuous removal of water azeotrophically for about 15 hours. After the reaction was complete, the reaction mixture was concentrated to a volume of 20-30 mL, quenched into dilute hydrochloric acid and chilled water (200 mL), and stirred for 60 minutes. The precipitated solid was filtered and dried to provide 30 g (95% yield, HPLC purity of 94% (including isomer)) of N,N-diethyl-2-cyano-3-(-3-ethoxy-4-hydroxy-5-nitrophenyl)acrylamide. The product was used as such directly to the next stage. MR=110.0-117.2° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07385072B2 |
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| Source dataset | uspto-grants-2008_06 |
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| ORD ID | ord-835738e53b76464a917b4f815a4aaf91 |
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| Source note | uspto-grants-2008_06 |
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