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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 38429Generated: October 23, 2026

Guanidine → 2-(4-Ethyl-7-methyl-benzo[b]thiophen-5-yloxy)-3-phenylamino-acrylonitrile

https://huagongshe.com/en/reaction/38429

Reaction equation

Participants

RoleNameHCIDCharge
ReactantGuanidineHCID 3520—
ReactantGuanidine HydrochlorideHCID 5742—
ReactantBenzenamine hydrochloride (1:1)HCID 8870—
ReactantSodium MethoxideHCID 10942334—
Reactant3,3-Bis-dimethylamino-2-(4-ethyl-7-methyl-benzo[b]thiophen-5-yloxy)-propionitrileHCID 59598706—
SolventEthanolHCID 702—
Product2-(4-Ethyl-7-methyl-benzo[b]thiophen-5-yloxy)-3-phenylamino-acrylonitrileHCID 6705341355%

Reaction Steps

3,3-Bis-dimethylamino-2-(4-ethyl-7-methyl-benzo[b]thiophen-5-yloxy)-propionitrile (590 mg, 2 mmol) and aniline HCl (1.1 g, 9 mmol) in 5 mL absolute ethanol were heated at reflux for 2.0 hours. In a separate flask, guanidine HCl (0.850 mg., 9 mmol) and sodium methoxide solution (1.83 ml, 9 mmol, 4.9 molar solution in methanol) were mixed in 1 ml Ethanol. The guanidine solution was added to the reaction mixture via pipette, and the reaction mixture was heated to reflux for 5 hours, then cooled. Solvent was removed in vacuo, and the residue was, chromatographed (5% MeOH/methylene chloride/1% Na4OH) to give 368 mg 2-(4-Ethyl-7-methyl-benzo[b]thiophen-5-yloxy)-3-phenylamino-acrylonitrile, 61%. Also present was 50 mg of 5-(4-Ethyl-7-methyl-benzo[b]thiophen-5-yloxy)-pyrimidine-2,4-diamine, 9%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08524725B2
Source datasetuspto-grants-2013_09
ORD IDord-cc4c99025821491089fd53ccd157da18
Source noteuspto-grants-2013_09