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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2083929Generated: November 1, 2026

Oxalyl chloride → N3-(5-Chlorothiophen-2-ylcarbonyl)-N2-[1-(4-pyridyl)piperidin-4-ylmethyl]-2,3-pyridinediamine

https://huagongshe.com/reaction/2083929

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
Reactant5-Chloro-2-thiophenecarboxylic acidHCID 95048—
ReactantN2-[1-(4-pyridyl)piperidin-4-ylmethyl]-2,3-pyridinediamineHCID 12150690—
SolventPyridineHCID 1049—
SolventChloroformHCID 6212—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductN3-(5-Chlorothiophen-2-ylcarbonyl)-N2-[1-(4-pyridyl)piperidin-4-ylmethyl]-2,3-pyridinediamineHCID 1299057262.3%

Reaction Steps

A solution of 5-chlorothiophene-2-carboxylic acid (120 mg, 0.72 mmol) in methylene chloride and DMF (0.005 mL) was treated with oxalyl chloride (0.105 mL, 1.20 mmol). After 0.25 h, the mixture was concentrated and the residue was dissolved in chloroform. This solution was added dropwise to a solution of N2-[1-(4-pyridyl)piperidin-4-ylmethyl]-2,3-pyridinediamine (170 mg, 0.6 mmol) in pyridine and chloroform. The reaction mixture was then purified using a procedure similar to that described in Example 2, Part D, yielding 160 mg (58%) of the title compound as a hydrochloride salt.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06716839B2
Source datasetuspto-grants-2004_04
ORD IDord-2aa0138a201a43748b6cab89c3acb2a9
Source noteuspto-grants-2004_04