HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethylamine hydrochloride → 6-chloro-N-ethyl-1-trityl-1H-pyrazolo[4,3-c]pyridin-3-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethylamine hydrochloride | HCID 11198 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | L-Proline | HCID 145742 | — |
| 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-ethyl-1-trityl-1H-pyrazolo[4,3-c]pyridin-3-amine | HCID 118272006 | — |
Reaction Steps
6-Chloro-3-iodo-1-trityl-1H-pyrazolo[4,3-c]pyridine (Intermediate 1C; 5.53 g, 10.60 mmol), proline (0.42 g, 3.65 mmol), copper (I) iodide (0.21 g, 1.103 mmol), potassium carbonate (7.40 g, 53.5 mmol), and ethylamine hydrochloride (2.78 g, 34.1 mmol) were stirred in DMSO (30 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-ethyl-1-trityl-1H-pyrazolo[4,3-c]pyridin-3-amine. MS ESI calc'd. For C27H23ClN4 [M+1]+ 439. found 439.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09233979B2 |
| Source dataset | uspto-grants-2016_01 |
| ORD ID | ord-b340ca210ebb4a15b375539f5f879250 |
| Source note | uspto-grants-2016_01 |