HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → N-benzyl-6-[1-(piperidin-4-yl)-1H-pyrazol-4-yl]-1H-pyrrolo[3,2-b]pyridin-1-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | tert-butyl 4-{4-[1-(benzylamino)-1H-pyrrolo[3,2-b]pyridin-6-yl]-1H-pyrazol-1-yl}piperidine-1-carboxylate | HCID 67458095 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | N-benzyl-6-[1-(piperidin-4-yl)-1H-pyrazol-4-yl]-1H-pyrrolo[3,2-b]pyridin-1-amine | HCID 58532480 | 51% |
Reaction Steps
A solution of tert-butyl 4-{4-[1-(benzylamino)-1H-pyrrolo[3,2-b]pyridin-6-yl]-1H-pyrazol-1-yl}piperidine-1-carboxylate (25 mg, 0.053 mmol) in MeOH (0.3 mL) was treated with HCl (4.0M solution in dioxane, 1.5 mL) at room temperature for 30 min. Solvents were evaporated and the residue was diluted with aq. NaHCO3, extracted with ethyl acetate. The organic layer was dried, filtered and evaporated to give a white solid (10 mg, yield 51%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08912330B2 |
| Source dataset | uspto-grants-2014_12 |
| ORD ID | ord-3791328c92394789b4478d2ac7a26b14 |
| Source note | uspto-grants-2014_12 |