HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 3-Amino-1-phenyl-1H-pyrazole-4-carbonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Phenylboronic Acid | HCID 66827 | — |
| Reactant | HCID 178510443 | HCID 178510443 | — |
| Catalyst | Cupric acetate | HCID 8895 | — |
| Product | 3-Amino-1-phenyl-1H-pyrazole-4-carbonitrile | HCID 2774249 | — |
| Product | 3-anilino-1-phenyl-1H-pyrazole-4-carbonitrile | HCID 67254303 | — |
Reaction Steps
3-amino-1H-pyrazole-4-carbonitrile (200 mg, 1.850 mmol), copper(II) acetate (504 mg, 2.78 mmol), phenylboronic acid (451 mg, 3.70 mmol) and pyridine (0.599 mL, 7.40 mmol) were stirred in DCM (20 mL) at room temperature overnight. 2 N HCl was added and the products extracted in EtOAc (×2). The combined organic extracts were washed with brine, dried over MgSO4 and concentrated in vacuo. Purification of the residue by MPLC (2-30% EtOAc-hexanes) gave 3-anilino-1-phenyl-1H-pyrazole-4-carbonitrile (A) as a yellow solid and 3-amino-1-phenyl-1H-pyrazole-4-carbonitrile (B) as a pale yellow solid. 5-amino-1-phenyl-1H-pyrazole-4-carbonitrile was also isolated.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08415346B2 |
| Source dataset | uspto-grants-2013_04 |
| ORD ID | ord-373c8816e2fb4293a7ec3800604d42b7 |
| Source note | uspto-grants-2013_04 |