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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 49843Generated: October 25, 2026

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

https://huagongshe.com/reaction/49843

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 numberUS06710057B2
Source datasetuspto-grants-2004_03
ORD IDord-0208a0524ee5473484eeef0ced84e59f
Source noteuspto-grants-2004_03