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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 448078Generated: October 30, 2026

3-Pyridinecarbonyl chloride, hydrochloride (1:1) → HCID 69166888, compound

https://huagongshe.com/reaction/448078

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Pyridinecarbonyl chloride, hydrochloride (1:1)HCID 88438—
Reactant3-Butyl-2,4,5-trimethylthiazol-3-ium iodideHCID 69165591—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
ProductHCID 69166888HCID 69166888—

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 nicotinoyl chloride hydrochloride (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 0.94 (t, 3 H) 1.36-1.46 (m, 2 H) 1.61-1.68 (m, 2 H) 2.19 (s, 3 H) 2.22 (s, 3 H) 4.07-4.12 (m, 2 H) 6.69 (s, 1 H) 7.68-7.78 (m, 1 H) 8.54-8.61 (m, 1 H) 8.72-8.80 (m, 1 H) 9.18-9.29 (m, 1 H); MS (ESI) m/z 289 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08481574B2
Source datasetuspto-grants-2013_07
ORD IDord-4228edca180a430db51b6f08ed8a8a0a
Source noteuspto-grants-2013_07