HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 482263Generated: October 27, 2026
HCID 19063877, compound → HCID 178485720, compound
https://huagongshe.com/reaction/482263
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 19063877 | HCID 19063877 | — |
| Reactant | 2-cyano-3-ethoxyacrylic acid N-methyl-N-(3-trifluoromethylphenyl)amide | HCID 53640287 | — |
| Reactant | HCID 178501943 | HCID 178501943 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 178485720 | HCID 178485720 | 77.7% |
Reaction Steps
3.60 g (=3.67 ml, 20 mmol) of 30% strength NaOCH3 /CH3OH solution were added to a solution of 4.74 g (20 mmol) of 1-amidino-4,4-dimethyl-2-oxoimidazolidine hydrobromide in 47 ml of methanol at room temperature, and the mixture was stirred at 45° C. for 30 min. The solution was then cooled to 20° C. and, at 20° C., 5.97 g (20 mmol) of 2-cyano-3-ethoxyacrylic acid N-methyl-N-(3-trifluoromethylphenyl)amide were added and the mixture was stirred at 20° C. for 20 min, at room temperature for 1.5 hours and while cooling in an icebath for 30 min. The solid which had separated out was filtered off with suction, washed with ether and worked up further as described in Example 1. Likewise, the residue from the filtrate (mother liquor) was further worked up as described in Example 1 and dried. 6.35 g (=77.7% yield) of, according to TLC (CH2Cl2 /C2H5 OH=10:1), virtually pure compound IV were obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05795899 |
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| Source dataset | uspto-grants-1998_08 |
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| ORD ID | ord-5a9461b0445d45339dfc96697416e4b4 |
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| Source note | uspto-grants-1998_08 |
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