HuagongsheHuagongshe Chemistry Print Report · For research reference only
Glycolic Acid → 2-Hydroxymethyl-5-methoxy-3-methylimidazo[5,4-b]pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Glycolic Acid | HCID 757 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Toluene | HCID 1140 | — |
| Reactant | 6-methoxy-2-N-methylpyridine-2,3-diamine | HCID 5743760 | — |
| Product | 2-Hydroxymethyl-5-methoxy-3-methylimidazo[5,4-b]pyridine | HCID 10821600 | — |
Reaction Steps
A solution of 2.20 g of 3-amino-6-methoxy-2-methylaminopyridine (prepared as described in Preparation 68) and 3.30 g of glycolic acid in 40 ml of toluene was heated under reflux for 4 hours. At the end of this time, the reaction mixture was poured into water, after which it was extracted with ethyl acetate. The extract was washed with an aqueous solution of sodium chloride and dried over anhydrous sodium sulfate, after which the solvent was removed by distillation under reduced pressure. The residue was purified by column chromatography through silica gel, using a 30:1 by volume mixture of ethyl acetate and methanol as the eluent, to give 620 mg of the title compound, melting at 138°-140° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05624935 |
| Source dataset | uspto-grants-1997_04 |
| ORD ID | ord-bb7602c650984fbe936f7527d0fac10c |
| Source note | uspto-grants-1997_04 |