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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 314Generated: October 23, 2026

5-(4-Methyl-1H-imidazol-1-yl)pyridin-2-amine → (R)-4-Methyl-N-(5-(4-methyl-1H-imidazol-1-yl)pyridin-2-yl)-2-phenyl-2,3,4,5-tetrahydropyrido[3,2-f][1,4]oxazepin-8-amine

https://huagongshe.com/en/reaction/314

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-(4-Methyl-1H-imidazol-1-yl)pyridin-2-amineHCID 57512861—
Reactant(2R)-8-chloro-4-methyl-2-phenyl-3,5-dihydro-2H-pyrido[3,2-f][1,4]oxazepineHCID 57512880—
ReagentCesium carbonateHCID 10796—
Catalyst2-(Dicyclohexylphosphino)biphenylHCID 2734216—
CatalystPalladium (II) acetateHCID 4144353—
Solvent1,2-DimethoxyethaneHCID 8071—
Product(R)-4-Methyl-N-(5-(4-methyl-1H-imidazol-1-yl)pyridin-2-yl)-2-phenyl-2,3,4,5-tetrahydropyrido[3,2-f][1,4]oxazepin-8-amineHCID 5751283235.89%

Reaction Conditions

Temperature100 °C

Reaction Steps

(R)-8-chloro-4-methyl-2-phenyl-2,3,4,5-tetrahydropyrido[3,2-f][1,4]oxazepine (129 mg, 0.47 mmol), 5-(4-methyl-1H-imidazol-1-yl)pyridin-2-amine (82 mg, 0.47 mmol), PALLADIUM(II) ACETATE (10.54 mg, 0.05 mmol), 2-(DICYCLOHEXYLPHOSPHINO)BIPHENYL (16.46 mg, 0.05 mmol) and Cs2CO3 (229 mg, 0.70 mmol) were weighed into a microwave vial which was capped and flushed with argon. DME (5 mL) was added and the mixture was heated to 100°C in a microwave apparatus for 2 h. The mixture was filtered and purified by column chromatography on Silica using gradient elution with increasing concentration of methanol, from 0 to 6 %, in dichloromethane to give(R)-4-methyl-N-(5-(4-methyl-1H-imidazol-1-yl)pyridin-2-yl)-2-phenyl-2,3,4,5-tetrahydropyrido[3,2-f][1,4]oxazepin-8-amine (69.5 mg, 35.9 %)

Provenance & Evidence

Source dataset750 AstraZeneca ELN dataset
ORD IDord-2bf055ae52c14e578ca506139e6af8cb
Source note750 AstraZeneca ELN dataset