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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 397544Generated: October 29, 2026

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

https://huagongshe.com/reaction/397544

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 numberUS06610704B1
Source datasetuspto-grants-2003_08
ORD IDord-116baf5411ef42248885d81115a452db
Source noteuspto-grants-2003_08