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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1370647Generated: November 2, 2026

Pyridine → N4-(tert-butyloxycarbonyl)-N3-(4-methoxybenzoyl)-3,4-pyridinediamine

https://huagongshe.com/reaction/1370647

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactantp-Anisoyl chlorideHCID 7477—
ReactantSodium HydroxideHCID 14798—
Reactant3-Amino-4-(Boc-amino)pyridineHCID 11095863—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductN4-(tert-butyloxycarbonyl)-N3-(4-methoxybenzoyl)-3,4-pyridinediamineHCID 1206953760.7%

Reaction Steps

A solution of N4-(tert-butyloxycarbonyl)-3,4-pyridinediamine (500 mg, 2.40 mmol) and pyridine (0.213 mL, 2.63 mmol) in methylene chloride (12 mL) was treated with p-anisoyl chloride (408 mg, 2.40 mmol). After 0.75 hr, the mixture was poured into a mixture of ethyl acetate and 1 N aqueous sodium hydroxide. The organic layer was washed with saturated sodium chloride, dried (magnesium sulfate), and filtered. Concentration in vacuo and recrystallization of the residue, followed by flash chromatography (silica gel, hexanes/ethyl acetate) yielded 500 mg (60%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06583173B2
Source datasetuspto-grants-2003_06
ORD IDord-cf69f3cd65ea429590355c4d9c06f89c
Source noteuspto-grants-2003_06