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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 384683Generated: October 29, 2026

Sodium Carbonate → N4-(1-Methylpiperidin-4-yl)-5-phenylpyridine-2,4-diamine

https://huagongshe.com/reaction/384683

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantPhenylboronic AcidHCID 66827—
ReactantN-(5-Chloro-4-(1-methylpiperidin-4-ylamino)pyridin-2-yl)pivalamideHCID 59613362—
SolventAcetonitrile--water (1/1)HCID 18373917—
ProductN4-(1-Methylpiperidin-4-yl)-5-phenylpyridine-2,4-diamineHCID 59613481238.6%

Reaction Conditions

Temperature130 °C

Reaction Steps

A solution of the N-(5-chloro-4-(1-methylpiperidin-4-ylamino)pyridin-2-yl)pivalamide (Synthesis 153-C) (0.187 g, 0.57 mmol), phenyl boronic acid (0.140 g, 1.15 mmol), sodium carbonate (0.153 g, 1.43 mmol) and Bedford catalyst (0.003 g, 0.005 mmol) in a mixture of acetonitrile/water (4/1, 3.1 mL) was heated under microwave irradiation for 30 min at 130° C. The crude reaction mixture was purified by ion exchange on SCX-II acidic resin (1 g) eluting with methanol/dichloromethane (1/1), then 2M ammonia-methanol. The basic fractions were combined and the solvent was removed in vacuo. The crude mixture was used without further purification. A solution of the protected amine in 6 M HCl (3 mL) was heated under microwave irradiation at 105° C. for 50 min. The solution was basified with Na2CO3 and extracted with ethyl acetate (3×10 mL). The crude mixture was purified by flash chromatography on silica, eluting with methanol and dichloromethane (1/9), to give the title compound as a colourless solid (0.384 g, 73%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367658B2
Source datasetuspto-grants-2013_02
ORD IDord-27287188ad464b74ad0cc519ff79a849
Source noteuspto-grants-2013_02