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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 448080Generated: October 29, 2026

2-Chloronicotinoyl chloride → HCID 86623756, compound

https://huagongshe.com/reaction/448080

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloronicotinoyl chlorideHCID 2774541—
Reactant3-Butyl-2,4,5-trimethylthiazol-3-ium iodideHCID 69165591—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
ProductHCID 86623756HCID 86623756—

Reaction Steps

In a 20 mL vial 3-butyl-2,4,5-trimethylthiazol-3-ium iodide (48 mg in 0.5 mL DMA, 0.16 mmol, 1 equiv.) was added, followed by TEA (38 mg in 0.5 mL DMA, 0.37 mmol, 2.4 equiv.) and the solution went black. DMAP (2 mg in 0.5 mL DMA, 0.016 mmol, 0.1 equiv) was added next, followed by 2-chloronicotinoyl chloride (0.9 mL of 0.2M in DMA, 1.2 equiv). The mixture was shaken overnight at room temperature and then concentrated in vacuo. The resulting residue was taken up in 1:1 DMSO/MeOH and purified by reverse phase HPLC using a method analogous to that described in Example 53 to provide the title compound. 1H NMR (500 MHz, DMSO-d6/D2O) δ ppm 0.91 (t, 3 H) 1.31-1.39 (m, 2 H) 1.58-1.67 (m, 2 H) 2.19 (s, 3 H) 2.21 (s, 3 H) 3.93-3.98 (m, 2 H) 6.15 (s, 1 H) 7.47 (dd, 1 H) 7.94 (dd, 1 H) 8.41 (dd, 1 H); MS (ESI) m/z 323 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08481574B2
Source datasetuspto-grants-2013_07
ORD IDord-c2392ac459c748f384156421a8d804aa
Source noteuspto-grants-2013_07