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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | N-(4-(3-chloropyrazin-2-yloxy)phenyl)pyridin-2-amine | HCID 53485989 | — |
| Reactant | HCID 178419772 | HCID 178419772 | — |
| Product | N-(4-(3-Benzylpyrazin-2-yloxy)phenyl)pyridin-2-amine | HCID 59374294 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08637500B2 |
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| Source dataset | uspto-grants-2014_01 |
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| ORD ID | ord-adeed2dc030f40139f78929909584496 |
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| Source note | uspto-grants-2014_01 |
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