HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl 6-chloropyridine-3-carboxylate → HCID 178498148, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl 6-chloropyridine-3-carboxylate | HCID 254249 | — |
| Reactant | Potassium Bicarbonate | HCID 516893 | — |
| Reactant | HCID 178419017 | HCID 178419017 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178498148 | HCID 178498148 | — |
Reaction Steps
0.5 g (4.5 mmol) of histamine and 0.77 g (4.5 mmol) of 6-chloro-3-carbomethoxypyridine are stirred with potassium bicarbonate in 20 ml of tetrahydrofuran at 21° C. for 24 h and then heated at reflux for 24 h. The mixture is evaporated and the white solid residue is chromatographed through silica gel, using a chloroform/methanol (4/1) mixture as eluent. The fractions containing the pure product are combined and evaporated and the resulting oily residue is treated with a methanol solution of oxalic acid. Addition of ether provides the title compound in the form of the oxalate salt, M.p.: 209°-210° C. C12H14N4O2.1.7C2H2O4
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | USRE037303E1 |
| Source dataset | uspto-grants-2001_07 |
| ORD ID | ord-7f4cb14dc5d74c6cb5b6d4c7f4e6cf3e |
| Source note | uspto-grants-2001_07 |