HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 844443Generated: October 30, 2026
Hydrochloric Acid → benzyl 1H-pyrrolo[3,2-c]pyridine-2-carboxylate
https://huagongshe.com/reaction/844443
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | tert-butyl N-(3-methylpyridin-4-yl)carbamate | HCID 15273533 | — |
| Reactant | Benzyloxalate | HCID 19738602 | — |
| Reactant | HCID 178418306 | HCID 178418306 | — |
| Solvent | Pentane | HCID 8003 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | benzyl 1H-pyrrolo[3,2-c]pyridine-2-carboxylate | HCID 22612567 | 44.6% |
Reaction Steps
40 ml of 1.7M tert-butyllithium in pentane are added, at −40° C. under nitrogen, to 5 g of 4-(N-Bocamino)-3-methylpyridine. After stirring for 1 hour at −40° C., the lithiated derivative thus formed is added to 12.9 g of benzyl oxalate in 100 ml of THF at −40° C. The mixture is allowed to return to 0° C., it is left stirring for 2 hours, 25 ml of 6N HCl are then added and this mixture is heated at 50° C. for one and a half hours. The pH is brought to 9 by addition of 1N NaOH, the mixture is then extracted with EtOAc and the extracts are dried and evaporated. The residue is chromatographed on silica, eluting with DCM/MeOR (100/3; v/v) to give 2.7 g of the expected compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06380230B1 |
|---|
| Source dataset | uspto-grants-2002_04 |
|---|
| ORD ID | ord-7407aa4c38a749dd8bf6c668938032d6 |
|---|
| Source note | uspto-grants-2002_04 |
|---|