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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 473638Generated: October 31, 2026

Hydrochloric Acid → N-(4-(3-Benzylpyrazin-2-yloxy)phenyl)pyridin-2-amine

https://huagongshe.com/reaction/473638

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTetrahydrofuranHCID 8028—
ReactantN-(4-(3-chloropyrazin-2-yloxy)phenyl)pyridin-2-amineHCID 53485989—
ReactantHCID 178419772HCID 178419772—
ProductN-(4-(3-Benzylpyrazin-2-yloxy)phenyl)pyridin-2-amineHCID 59374294—

Reaction Conditions

Temperature70 °C

Reaction Steps

A suspension of N-(4-(3-chloropyrazin-2-yloxy)phenyl)pyridin-2-amine (200 mg, 0.670 mmol), benzylzinc bromide, 0.5M in THF (6.7 mL, 3.35 mmol), and bis(di-t-butyl(4-dimethylaminophenyl)phosphine)dichloropalladium(II) (80 mg, 0.11 mmol) was sparged with argon for 5 minutes then heated to 70° C. for 2 h. The reaction was then partitioned between EtOAc (30 mL) and sat NH4Cl (10 mL). The separated organic layer was dried over MgSO4, concentrated under reduced pressure, then purified on silica (40 g) eluting with 1.5-2.0% MeOH/DCM. The resulting residue was then dissolved in MeOH (5 mL) and 0.105 mL of HCl (5 M; 0.105 mL, 0.525 mmol) added. The resulting solid was isolated by filtration to give the title compound. MS (ESI positive ion) m/z: 355.1 (M+1). IC50 (uM) 0.250.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08637500B2
Source datasetuspto-grants-2014_01
ORD IDord-adeed2dc030f40139f78929909584496
Source noteuspto-grants-2014_01