HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 879647Generated: October 30, 2026
1-Methylpiperazine → HCID 86700459, compound
https://huagongshe.com/reaction/879647
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Methylpiperazine | HCID 53167 | — |
| Reactant | L-Proline | HCID 145742 | — |
| Reactant | HCID 86700460 | HCID 86700460 | — |
| Reactant | HCID 86700461 | HCID 86700461 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Product | HCID 86700459 | HCID 86700459 | — |
Reaction Steps
To a solution of 5-chloro-3-iodo-1-methyl-1H-pyrazolo[4,3-b]pyridine (104 mg, 0.354 mmol, containing the isomer 5-chloro-3-iodo-2-methyl-2H-pyrazolo[4,3-b]pyridine (360 mg, 1.22 mmol) was added 1-methylpiperazine (184 mg, 1.84 mmol), CuI (70 mg, 0.368 mmol), L-proline (84 mg, 0.736 mmol). The reaction mixture was heated at 100° C. for 4 h. The reaction was cooled, washed by sat. NaHCO3, extracted with EtOAc, dried over MgSO4, filtered, concentrated and purified by silica gel column, eluting by 0-100% EtOAc in hexanes to give the product. LCMS-ESI+: calc'd for C12H16ClN5: 266.1 (M+H+); Found: 266.2 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08987250B2 |
|---|
| Source dataset | uspto-grants-2015_03 |
|---|
| ORD ID | ord-dea244862039419495a0a5aae9001ec3 |
|---|
| Source note | uspto-grants-2015_03 |
|---|