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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 482263Generated: October 27, 2026

HCID 19063877, compound → HCID 178485720, compound

https://huagongshe.com/reaction/482263

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 19063877HCID 19063877—
Reactant2-cyano-3-ethoxyacrylic acid N-methyl-N-(3-trifluoromethylphenyl)amideHCID 53640287—
ReactantHCID 178501943HCID 178501943—
SolventMethanolHCID 887—
ProductHCID 178485720HCID 17848572077.7%

Reaction Conditions

Temperature45 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05795899
Source datasetuspto-grants-1998_08
ORD IDord-5a9461b0445d45339dfc96697416e4b4
Source noteuspto-grants-1998_08