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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2182815Generated: November 1, 2026

Pyridine-4-carbonyl chloride → HCID 10149810, compound

https://huagongshe.com/reaction/2182815

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridine-4-carbonyl chlorideHCID 417436—
Reactant(4-chlorophenyl)(1-methyl-1H-pyrrol-2-yl)methanoneHCID 1116388—
ReactantAluminum(III) ChlorideHCID 6451240—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 10149810HCID 1014981027%

Reaction Steps

A solution of 17.5 g (0.08 mole) of (4-chlorophenyl)(1-methyl-1H-pyrrol-2-yl)methanone, 14.4 g (0.088 mole) of isonicotinoyl chloride and 26.6 g of aluminum chloride (0.2 mole) in 280 mL of DCE was heated under reflux for 16 h. After cooling, the mixture was partitioned between CH2Cl2 and dilute NaOH solution. The organic layer was dried and the solvent was evaporated in vacuo. The residue was triturated with ether. The resulting solid was recrystallized from 2-PrOH to give 7 g (27%) of the title compound, mp 174-175° C. ES-MS m/z=325 (M++H). 1H NMR (300 MHz, CDCl3) δ 4.1 (s, 3H); 7.1 (s, 1H); 7.3(dd, 2H); 7.42 (dd, 2H); 7.45 (s, 1H); 7.8 (dd, 2H); 8.8 (dd, 2H). Anal calc'd for: C18H13ClN2O2: C, 66.57; H, 4.03; N, 8.63. Found: C, 66.34; H, 3.94; N, 8.53.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06897319B2
Source datasetuspto-grants-2005_05
ORD IDord-5a3277f175fb41649eaadafccc6cb043
Source noteuspto-grants-2005_05