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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 333557Generated: October 30, 2026

3-Iodo-N-methylpyridin-2-amine → HCID 68205837, compound

https://huagongshe.com/reaction/333557

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Iodo-N-methylpyridin-2-amineHCID 14047146—
ReactantHCID 21735431HCID 21735431—
ReactantSodium t-butoxideHCID 23676156—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
Catalyst2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenylHCID 11155794—
SolventTolueneHCID 1140—
ProductHCID 68205837HCID 6820583791%

Reaction Conditions

Temperature120 °C

Reaction Steps

A 1 L round-bottomed flask was charged with 3-iodo-N-methylpyridin-2-amine (8.95 g, 38.3 mmol), N1,N1-diphenylbenzene-1,3-diamine (9.96 g, 38.3 mmol), dicyclohexyl(2′,4′,6′-triisopropyl-[1,1′-biphenyl]-2-yl)phosphine (0.183 g, 0.384 mmol) and sodium 2-methylpropan-2-olate (5.15 g, 53.6 mmol) in toluene (500 mL). Nitrogen was bubbled through for 10 minutes. Then Pd2 dba3 (88 mg, 0.10 mmol) was added and this was stirred at 120° C. for overnight. The mixture was then filtered and the filtrate was concentrated and chromatographed using a mobile phase gradient of 0-20% ethyl acetate in dichloromethane to give N3-(3-(diphenylamino)phenyl)-N2-methylpyridine-2,3-diamine (12.2 g, 91% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08883322B2
Source datasetuspto-grants-2014_11
ORD IDord-828736f310194f469037dceba4446170
Source noteuspto-grants-2014_11