HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 21948152, compound → HCID 10223719, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 21948152 | HCID 21948152 | — |
| Reactant | HCID 178418336 | HCID 178418336 | — |
| Catalyst | HCID 178418745 | HCID 178418745 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 10223719 | HCID 10223719 | 41% |
Reaction Steps
To a solution of 2-anilino-7-chloro-5-methyl-1-phenyl-1,8-naphthyridin-4(1H)-one (100 mg, 0.277 mmol) in THF was added Ni(dppp)Cl2 (37.0 mg, 0.069 mmol). After stirring for 5 min, benzylmagnesium chloride (2M, 1.45 mL, 2.90 mmol) was added dropwise via syringe and the mixture was allowed to stir for 24 h. The mixture was quenched with 1 N HCl and extracted with EtOAc. The organic layer was washed brine, dried over MgSO4, and concentrated in vacuo. Purification by preparative HPLC (10% MeNC in water with 0.1% TFA to 95% CH3CN in water, 10 mL/min, 10 min) provided 2-anilino-7-benzyl-5-methyl-1-phenyl-1,8-naphthyridin-4(1H)-one (47.3 mg, 41%): LCMS RT: 2.85 min, MH+: 418.3.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06964971B2 |
| Source dataset | uspto-grants-2005_11 |
| ORD ID | ord-c5578776cdca451ea6af12e1679fbc58 |
| Source note | uspto-grants-2005_11 |