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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1455689Generated: November 1, 2026

Pyridine → HCID 18440729, compound

https://huagongshe.com/reaction/1455689

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant5-Chlorothiophene-2-carbonyl ChlorideHCID 589223—
ReactantHCID 18440731HCID 18440731—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventTetrahydrofuranHCID 8028—
ProductHCID 18440729HCID 18440729—

Reaction Steps

At 0° C., 0.97 g (5.35 mmol) of 5-chlorothiophene-2-carbonyl chloride is added dropwise to a suspension of 1.48 g (4.12 mmol) of tert-butyl 4-[2-(4-amino-1-oxo-1,3-dihydro-2H-isoindol-2-yl) ethyl]-1-piperidinecarboxylate, 1.7 ml (20.6 mmol) of pyridine and 25 mg (0.206 mmol) of 4-DMAP in 21 ml of absolute THF. The mixture is slowly warmed to room temperature and stirred overnight. The reaction mixture is concentrated and then separated by chromatography on silica gel (dichloromethane/methanol 97:3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07482472B2
Source datasetuspto-grants-2009_01
ORD IDord-35ec79318d114603b51284cc5b07174f
Source noteuspto-grants-2009_01