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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1094789Generated: October 25, 2026

Pentane → 3-(2-Chloro-5-methoxyphenyl)pyridine-2,6-diamine

https://huagongshe.com/reaction/1094789

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPentaneHCID 8003—
ReactantCesium carbonateHCID 10796—
Reactant3-Iodopyridine-2,6-diamineHCID 476218—
Reactant(2-Chloro-5-methoxyphenyl)boronic acidHCID 17750233—
CatalystTetrakis(triphenylphosphine)palladiumHCID 11979704—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
Product3-(2-Chloro-5-methoxyphenyl)pyridine-2,6-diamineHCID 57582341109%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a suspension of 3-iodopyridine-2,6-diamine (Preparation 44, 2 g, 8.51 mmol) in 1,4-dioxane (10 ml) and water (5 ml) was added 2-chloro-5-methoxyphenyl boronic acid (0.793 g, 4.25 mmol), cesium carbonate (2.77 g, 8.51 mmol) and palladium tetrakis(triphenylphosphine) (0.123 g, 0.0125 mmol). The reaction was purged with nitrogen and heated at 80° C. for 20 minutes. Three further portions of palladium tetrakis(triphenylphosphine) (0.123 g, 0.0125 mmol) and 2-chloro-5-methoxyphenyl boronic acid (0.793 g, 4.25 mmol) were added at 20 minute intervals. The reaction was heated at 80° C. for 18 hours before concentrating in vacuo. The residue was taken up in ethyl acetate (20 ml) and washed with a saturated aqueous solution of brine (20 ml) before drying over Na2SO4 and concentrating in vacuo. The residue was purified by silica gel column chromatography, eluting with 50:50 to 100:0 ethyl acetate:pentane to afford the title compound as a brown foam (1.157 g, 55% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08134007B2
Source datasetuspto-grants-2012_03
ORD IDord-d20b20bb5df8404abc3c510ea048878b
Source noteuspto-grants-2012_03