Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 62502Generated: October 30, 2026

Potassium Phosphate, Tribasic → 2-[(2,5-dichloro-4-pyridinyl)amino]-N-(methyloxy)benzamide

https://huagongshe.com/reaction/62502

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant2-Amino-N-methoxybenzamideHCID 12392707—
Reactant2,5-Dichloro-4-iodopyridineHCID 53400965—
Catalystpalladium(II) acetateHCID 167845—
CatalystBis[2-(diphenylphosphino)phenyl] etherHCID 4285986—
Solvent1,4-DioxaneHCID 31275—
Product2-[(2,5-dichloro-4-pyridinyl)amino]-N-(methyloxy)benzamideHCID 5751689687.5%

Reaction Conditions

Temperature110 °C

Reaction Steps

A mixture of 2,5-dichloro-4-iodo-pyridine (40 g, 146.5 mmole, 1 eq), 2-amino-N-methoxy-benzamide (24.32 g, 146.5 mmole, 1 eq) and K3PO4 (77.72 g 366.2 mmole, 2.5 eq) in 1,4-dioxane (600 mL) was degassed with N2 for 1 h. To this were added Pd(OAc)2 (0.657 g, 2.93 mmole, 0.02 eq), DPEPhos (6.31 g, 11.7 mmole, 0.08 eq) and again degassed for 15 min with N2. The resulting mixture was stirred at 110° C. for overnight. After completion of reaction, solid material was collected by filtration, dissolved in water (500 mL) and extracted with ethyl acetate (5×200 mL). Combined organic layer was dried over sodium sulfate, filtered and concentrated under reduced pressure. Solid compound so obtained was purified by washing with hexane to give the title compound as yellowish solid (40 g, 53%). 1H-NMR (400 MHz, DMSO-d6): δ 3.63 (s, 3H), 7.06 (s, 1H), 7.15-7.22 (m, 1H), 7.48-7.57 (m, 2H), 7.66-7.67 (d, 1H, J=7.48 Hz), 8.25 (s, 1H), 10.66-11.45 (brs, 1H). LC-MS [M+H]+=312.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09446034B2
Source datasetuspto-grants-2016_09
ORD IDord-c9e09b0554cb4812a5d43ba4fb268a88
Source noteuspto-grants-2016_09