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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1961507Generated: October 26, 2026

Hydrochloric Acid → 3-Amino-1-phenyl-1H-pyrazole-4-carbonitrile

https://huagongshe.com/reaction/1961507

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPyridineHCID 1049—
ReactantDichloromethaneHCID 6344—
ReactantPhenylboronic AcidHCID 66827—
ReactantHCID 178510443HCID 178510443—
CatalystCupric acetateHCID 8895—
Product3-Amino-1-phenyl-1H-pyrazole-4-carbonitrileHCID 2774249—
Product3-anilino-1-phenyl-1H-pyrazole-4-carbonitrileHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08415346B2
Source datasetuspto-grants-2013_04
ORD IDord-373c8816e2fb4293a7ec3800604d42b7
Source noteuspto-grants-2013_04