HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Carbonate → 6-chloro-N-methyl-1-trityl-1H-pyrazolo[4,3-c]pyridin-3-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | L-Proline | HCID 145742 | — |
| Reactant | Methylamine hydrochloride | HCID 6364545 | — |
| Reactant | 6-Chloro-3-iodo-1-trityl-1H-pyrazolo[4,3-c]pyridine | HCID 89525858 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 6-chloro-N-methyl-1-trityl-1H-pyrazolo[4,3-c]pyridin-3-amine | HCID 118272406 | — |
Reaction Steps
6-Chloro-3-iodo-1-trityl-1H-pyrazolo[4,3-c]pyridine (Intermediate 1C; 6.08 g, 11.65 mmol), proline (0.42 g, 3.65 mmol), copper(I) iodide (0.24 g, 1.260 mmol), potassium carbonate (9.83 g, 71.1 mmol), and methylamine hydrochloride (3.26 g, 48.3 mmol) were stirred in DMSO (45 mL) at 70° C. for 24 h. Room temperature was attained, ammonium hydroxide was added, and the products extracted into DCM (×2). The combined organic extracts were washed with brine, dried over MgSO4, filtered, and concentrated in vacuo. Purification of the residue by flash chromatography (6-50% EtOAc-hexanes) gave 6-chloro-N-methyl-1-trityl-1H-pyrazolo[4,3-c]pyridin-3-amine MS ESI calc'd. For C26H21ClN4 [M+1]+ 425. found 425.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09233979B2 |
| Source dataset | uspto-grants-2016_01 |
| ORD ID | ord-48ce9db52e794b63a99f20805e6b577c |
| Source note | uspto-grants-2016_01 |