HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 2-Hydroxymethyl-1-methylimidazo[4,5-c]pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 2-t-Butyldimethylsilyloxymethyl-1-methylimidazo[4,5-c]pyridine | HCID 23298340 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Hydroxymethyl-1-methylimidazo[4,5-c]pyridine | HCID 23298368 | 111.6% |
Reaction Steps
A solution of 3.00 g of 2-t-butyldimethylsilyloxymethyl-1-methyl-1H-imidazo[4,5-c]pyridine (prepared as described in Preparation 72) in 60 ml of a 1:1: 1 by volume mixture of tetrahydrofuran, acetic acid and water was stirred at room temperature for 1 hour and then at 60° C. for 5 hours. At the end of this time, the reaction mixture was freed from the solvent by distillation. The resulting residue was mixed with an aqueous solution of sodium hydrogencarbonate and then concentrated by evaporation under reduced pressure. The concentrate was purified by column chromatography through silica gel, using a 10:1 by volume mixture of ethyl acetate and methanol as the eluent, to give 1.97 g of the title compound, melting at 285°-290° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05624935 |
| Source dataset | uspto-grants-1997_04 |
| ORD ID | ord-c53905f6dd084bb1b6cf06d89b5d796f |
| Source note | uspto-grants-1997_04 |