Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2107616Generated: October 30, 2026

O-Toluidine → Ethyl 3-methyl-7-(2-methylphenylamino)thieno[3,2-b]-pyridine-6-carboxylate

https://huagongshe.com/reaction/2107616

Reaction equation

Participants

RoleNameHCIDCharge
ReactantO-ToluidineHCID 7242—
ReactantEthyl 3-methyl-7-chlorothieno[3,2-b)pyridine-6-carboxylateHCID 23046143—
SolventAnisoleHCID 7519—
ProductEthyl 3-methyl-7-(2-methylphenylamino)thieno[3,2-b]-pyridine-6-carboxylateHCID 23046138—

Reaction Steps

Ethyl 3-methyl-7-chlorothieno[3,2-b]pyridine-6-carboxylate (3.0 g, 0.0117 mol) and o-toluidine (2.51 g, 0.0234 mol) in anisole (30 ml) were heated under reflux for three hours. The solvent was evaporated under reduced pressure, taken up in chloroform and washed in turn with 2NHCl, H2O, aqNa2CO3, H2O and brine, dried and evaporated to give an oil. This oil was purified by flash chromatography (silica, 40-60 mesh) using dichloromethane as eluant to give a buff coloured solid. This was crystallised from methanol to give the title compound, 2.3 g, m.p. 132°-134°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04935431
Source datasetuspto-grants-1990_06
ORD IDord-bbf6de0c19bb4bee96ccb0f90aab53b8
Source noteuspto-grants-1990_06