Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 325Generated: October 28, 2026

1-(3-Aminophenyl)-N,N-dimethyl-3-pyrrolidinamine → US9701664, Example 125

https://huagongshe.com/reaction/325

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(3-Aminophenyl)-N,N-dimethyl-3-pyrrolidinamineHCID 58529223—
Reactant6-chloro-N-[5-(2,3-dihydro-1,4-benzodioxine-6-carbonylamino)-2-methylphenyl]pyridine-3-carboxamideHCID 122585542—
ReagentSodium t-butoxideHCID 23676156—
Catalyst1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventTolueneHCID 1140—
ProductUS9701664, Example 125HCID 11799655010.22%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 6-chloro-N-(5-(2,3-dihydrobenzo[b][1,4]dioxine-6-carboxamido)-2-methylphenyl)nicotinamide (70 mg, 0.17 mmol),[Reactants],(9,9-dimethyl-9H-xanthene-4,5-diyl)bis(diphenylphosphine) (5.73 mg, 9.91 µmol),TRIS(DIBENZYLIDENEACETONE)DIPALLADIUM(0) (4.54 mg, 4.95 µmol),sodium 2-methylpropan-2-olate (23.81 mg, 0.25 mmol) in toluene (4 mL)/IPA (1.000 mL)was degassed with nitrogen and heated at reflux for 18 hours.The reaction mixture was filtered and filtered solid washed with ethyl acetate. The organic filtrate was washed with water (50ml), and organic layer dried over Na2SO4, filtered and evaporated.The crude product was purified by preparative HPLC (Waters XBridge Prep C18 OBD column, 5µ silica, 19 mm diameter, 100 mm length), using decreasingly polar mixtures of water (containing 1% NH3) and MeCN as eluents. Fractions containing the desired compound were evaporated to dryness to afford N-(5-(2,3-dihydrobenzo[b][1,4]dioxine-6-carboxamido)-2-methylphenyl)-6-(3-(3-(dimethylamino)pyrrolidin-1-yl)phenylamino)nicotinamide (10.00 mg, 10.22 %) as a cream solid.

Provenance & Evidence

Source dataset750 AstraZeneca ELN dataset
ORD IDord-68539516fcd24378954aa9ca9f44991e
Source note750 AstraZeneca ELN dataset