HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1593774Generated: October 31, 2026
Ethyl orthoformate → 2-cyano-N-(2,4-dichloro-5-methoxyphenyl)-3-{[3-iodo-4-(2-methoxyethoxy)phenyl]amino}acrylamide
https://huagongshe.com/reaction/1593774
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl orthoformate | HCID 31214 | — |
| Reactant | 2-cyano-N-(2,4-dichloro-5-methoxyphenyl)acetamide | HCID 16099178 | — |
| Reactant | 3-Iodo-4-(2-methoxyethoxy)aniline | HCID 66094206 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | 2-cyano-N-(2,4-dichloro-5-methoxyphenyl)-3-{[3-iodo-4-(2-methoxyethoxy)phenyl]amino}acrylamide | HCID 69312318 | 78.9% |
Reaction Steps
A suspension of 2-cyano-N-(2,4-dichloro-5-methoxyphenyl)acetamide (3.2 g, 12.4 mmol) and [3-iodo-4-(2-methoxyethoxy)phenyl]amine (4.0 g, 13.7 mmol) in 350 mL of iso-propanol was heated to reflux and triethylorthoformate (5.6 mL, 33.7 mmol) was added dropwise. The reaction mixture was heated at reflux for 3 hours. Additional triethylorthoformate (2.0 mL, 12.0 mmol) was added dropwise and the reaction mixture was heated at reflux overnight. The mixture was allowed to cool to room temperature and the solid was collected by filtration, washed with iso-propanol, diethyl ether, and ethyl acetate and then dried in vacuo to give 5.5 g of 2-cyano-N-(2,4-dichloro-5-methoxyphenyl)-3-{[3-iodo-4-(2-methoxyethoxy)phenyl]amino}acrylamide as a yellow solid, mp 209-210° C.; MS (ES) 560.0, 562.1 (M−H)−
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07297795B2 |
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| Source dataset | uspto-grants-2007_11 |
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| ORD ID | ord-91a3f71283404d0bac78272c45df537c |
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| Source note | uspto-grants-2007_11 |
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