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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 643Generated: October 23, 2026

4-Methoxybenzylamine → 4-N-[(4-methoxyphenyl)methyl]-2-N-phenylpyridine-2,4-diamine

https://huagongshe.com/en/reaction/643

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethoxybenzylamineHCID 75452—
Reactant4-chloro-N-phenylpyridin-2-amineHCID 23458041—
ReagentSodium t-butoxideHCID 23676156—
CatalystPalladium (II) acetateHCID 4144353—
Catalyst(R)-(-)-1-[(S)-2-(Dicyclohexylphosphino)ferrocenyl]ethyldi-t-butylphosphine;Ferrocene, 1-[(1R)-1-[bis(1,1-dimethylethyl)phosphino]ethyl]-2-(dicyclohexylphosphino)-, (2R)-HCID 144543273—
SolventDimethylacetamideHCID 31374—
Product4-N-[(4-methoxyphenyl)methyl]-2-N-phenylpyridine-2,4-diamineHCID 10188369267.69%

Reaction Conditions

Temperature100 °C

Reaction Steps

(4-methoxyphenyl)methanamine (73.7 mg, 0.54 mmol), 4-chloro-N- phenylpyridin-2-amine (100 mg, 0.49 mmol) and sodium 2-methylpropan-2-olate (94 mg, 0.98 mmol) were suspended in DMA (2 mL) and sealed into a microwave tube. Nitrogen was bubbled through the reaction mixture for 5 minutes. (R)-(-)-1-[(S)-2-(DICYCLOHEXYLPHOSPHINO)FERROCENYL]ETHYLDI-T-BUTYLPHOSPHINE (32.5 mg, 0.06 mmol) and diacetoxypalladium (8.78 mg, 0.04 mmol) were added to the reaction mixture and nitrogen was bubbled through the reaction mixture for a further 5 minutes. The reaction was heated thermally to 100 °C for 30 mins under nitrogen and cooled to RT. The reaction mixture was neutralised with HCl and purified by ion exchange chromatography, using a 20 g SCX column. The crude product was purified by flash silica chromatography, elution gradient 0 to 10% MeOH in DCM. Fractions containing product were evaporated to dryness to afford N4-(4-methoxybenzyl)-N2-phenylpyridine-2,4-diamine (101 mg, 67.7 %) as a white solid.

Provenance & Evidence

Source dataset750 AstraZeneca ELN dataset
ORD IDord-59c6d21cb6354f44a2ed185cff3caeb9
Source note750 AstraZeneca ELN dataset