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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1961507Erstellt: 27. Oktober 2026

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

https://huagongshe.com/reaction/1961507

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktPyridineHCID 1049—
EduktDichloromethaneHCID 6344—
EduktPhenylboronic AcidHCID 66827—
EduktHCID 178510443HCID 178510443—
KatalysatorCupric acetateHCID 8895—
Produkt3-Amino-1-phenyl-1H-pyrazole-4-carbonitrileHCID 2774249—
Produkt3-anilino-1-phenyl-1H-pyrazole-4-carbonitrileHCID 67254303—

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08415346B2
Quelldatensatzuspto-grants-2013_04
ORD IDord-373c8816e2fb4293a7ec3800604d42b7
Quellennotizuspto-grants-2013_04