Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1370652Generated: October 30, 2026

Sodium Hydroxide → N4-(tert-butyloxycarbonyl)-N3-[4-(4-pyridyl)benzoyl]-3,4-pyridinediamine

https://huagongshe.com/reaction/1370652

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantOxalyl chlorideHCID 65578—
Reactant3-Amino-4-(Boc-amino)pyridineHCID 11095863—
ReactantSodium 4-(pyridin-4-yl)benzoateHCID 23673507—
SolventPyridineHCID 1049—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductN4-(tert-butyloxycarbonyl)-N3-[4-(4-pyridyl)benzoyl]-3,4-pyridinediamineHCID 1206954410%

Reaction Steps

A suspension of sodium 4-(4-pyridyl)benzoate (425 mg, 1.92 mmol) in methylene chloride was treated with oxalyl chloride (0.840 mL, 9.60 mmol), followed by dimethylformamide (0.01 mL)). After 0.75 h, the mixture was concentrated in vacuo. The residue was then dissolved in methylene chloride and added dropwise to a solution of N4-(tert-butyloxycarbonyl)-3,4-pyridinediamine (400 mg, 1.92 mmol) and pyridine (0.31 mL) in methylene chloride (2 mL) and tetrahydrofuran (1 mL). After 16 h, the mixture was poured into ethyl acetate and 1 N aqueous sodium hydroxide. The organic layer was washed once with 1 N aqueous sodium hydroxide, once with saturated sodium chloride solution, dried (potassium carbonate), and filtered. The residue was purified by flash chromatography (silica gel, ethyl acetate/hexanes) to yield 75 mg (10%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06583173B2
Source datasetuspto-grants-2003_06
ORD IDord-3ee8b9d9b86540bda4e9152f046e212f
Source noteuspto-grants-2003_06