HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzylamine → Ethyl 3-methyl-7-benzylaminothieno[3,2-b]pyridine-6-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzylamine | HCID 7504 | — |
| Reactant | Ethyl 3-methyl-7-chlorothieno[3,2-b)pyridine-6-carboxylate | HCID 23046143 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | Ethyl 3-methyl-7-benzylaminothieno[3,2-b]pyridine-6-carboxylate | HCID 23046158 | — |
Reaction Steps
Ethyl 3-methyl-7-chlorothieno[3,2-b)pyridine-6-carboxylate (3.0 g, 0.0117 mol) and benzylamine (2.5 g, 0.0234 mol) were heated in an oil-bath with stirring for 30 minutes (oil-bath temperature to 220°). On cooling the residue was dissolved in chloroform, washed with dilute aqueous sodium hydroxide and the aqueous phase back-extracted with more chloroform. The combined chloroform extracts were washed with water, dried and evaporated to give an oil. This oil was purified by flash chromatography on silica (40-60 mesh) with dichloromethane as eluant to give an oil which crystallised on standing. Recrystallisation from methanol gives the title compound as pale yellow crystals, 3.0 g, m.p. 99°-100°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04935431 |
| Source dataset | uspto-grants-1990_06 |
| ORD ID | ord-613ade682fc14acea109e2237a55adf9 |
| Source note | uspto-grants-1990_06 |