HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1677345Generated: October 25, 2026
Guanidine → 2-(4-Ethyl-7-methyl-benzo[b]thiophen-5-yloxy)-3-phenylamino-acrylonitrile
https://huagongshe.com/reaction/1677345
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Guanidine | HCID 3520 | — |
| Reactant | Guanidine Hydrochloride | HCID 5742 | — |
| Reactant | Benzenamine hydrochloride (1:1) | HCID 8870 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | 3,3-Bis-dimethylamino-2-(4-ethyl-7-methyl-benzo[b]thiophen-5-yloxy)-propionitrile | HCID 59598706 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-(4-Ethyl-7-methyl-benzo[b]thiophen-5-yloxy)-3-phenylamino-acrylonitrile | HCID 67053413 | 55% |
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% NH4OH) 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08008313B2 |
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| Source dataset | uspto-grants-2011_08 |
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| ORD ID | ord-27b32d90e1c44281b3c1bf9a0f23ef32 |
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| Source note | uspto-grants-2011_08 |
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