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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 267Generated: October 23, 2026

4-Amino-2-methoxybenzonitrile → (R)-4-(4-(2-Hydroxyethyl)-2-phenyl-2,3,4,5-tetrahydropyrido[3,2-f][1,4]oxazepin-8-ylamino)-2-methoxybenzonitrile

https://huagongshe.com/en/reaction/267

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Amino-2-methoxybenzonitrileHCID 232735—
Reactant(R)-2-(8-chloro-2-phenyl-2,3-dihydropyrido[3,2-f][1,4]oxazepin-4(5H)-yl)ethanolHCID 59577824—
ReagentCesium carbonateHCID 10796—
Catalyst2-(Dicyclohexylphosphino)biphenylHCID 2734216—
CatalystPalladium (II) acetateHCID 4144353—
Solvent1,2-DimethoxyethaneHCID 8071—
Product(R)-4-(4-(2-Hydroxyethyl)-2-phenyl-2,3,4,5-tetrahydropyrido[3,2-f][1,4]oxazepin-8-ylamino)-2-methoxybenzonitrileHCID 4981878713.17%

Reaction Conditions

Temperature100 °C

Reaction Steps

4-amino-2-methoxybenzonitrile (72.9 mg, 0.49 mmol), (R)-2-(8-chloro-2-phenyl-2,3-dihydropyrido[3,2-f][1,4]oxazepin-4(5H)-yl)ethanol (150 mg, 0.49 mmol), Palladium acetate (11.05 mg, 0.05 mmol), 2-(Dicyclohexylphosphino)biphenyl (17.25 mg, 0.05 mmol)and Cesium carbonate (481 mg, 1.48 mmol) were added to a microwave vial. 1,2-dimethoxyethane (2 mL) and EtOH (0.500 mL) were added. The reaction mixture was flushed with argon and the mixture was run in a microwave for 60 minutes at 100°C. The solvent was decanted and the solids were washed with 5ml DCM. The solvent was evaporated and the crude product was purified on Si, 0-6% MeOH in DCM, yielding (R)-4-(4-(2-hydroxyethyl)-2-phenyl-2,3,4,5-tetrahydropyrido[3,2-f][1,4]oxazepin-8-ylamino)-2-methoxybenzonitrile (27.0 mg, 13.17 %)

Provenance & Evidence

Source dataset750 AstraZeneca ELN dataset
ORD IDord-7d01f29fd6fc44f08392db2774553827
Source note750 AstraZeneca ELN dataset