Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 605885Generated: October 30, 2026

Benzoyl chloride → HCID 131724857, compound

https://huagongshe.com/reaction/605885

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantSodium CarbonateHCID 10340—
ReactantDimethylacetamideHCID 31374—
Reactant2,6-Dichloro-3-pyridylamineHCID 112846—
Catalystpalladium(II) acetateHCID 167845—
SolventDichloromethaneHCID 6344—
ProductHCID 131724857HCID 13172485713%

Reaction Conditions

Temperature125 °C

Reaction Steps

Amide 5 was prepared from commercial reagents, benzoyl chloride and 3-amino-2,6-dichloropyridine in DCM in high yield. The desired product 4g was prepared by dissolving amide 5 (4.45 g, 16.7 mmol) in DMA (35 mL) and adding sodium carbonate (1.8 g, 16.7 mmol) and palladium acetate (400 mg, catalytic amt.). The reaction mixture was heated to 125° C. for several hours until the stating material was no longer present by TLC. The reaction was then cooled down to room temperature and concentrated in vacuo and the crude residue was suspended in boiling EtOAc (100 mL) and filtered through a plug of celite. The filtrate was concentrated and the solid that precipitated out was filtered off and determined to be compound 4g (520 mg, 13% yield). Mp=285-295 (dec.) ° C.; 1H NMR (d6-DMSO) δ 11.92 (bs, 1H), 8.62 (d, 1H), 8.32 (d, 1H), 7.95 (t, 1H), 7.77 (m, 2H), 7.62 (d, 1H). Anal Calcd. for C12H7ClN2O: C, 62.49; H, 3.06; N, 12.15. Found: C, 61.40; H, 3.19; N, 11.77.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07915280B2
Source datasetuspto-grants-2011_03
ORD IDord-c1c0117d5a3647f49a6c4ec290315969
Source noteuspto-grants-2011_03