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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 311Generated: October 25, 2026

6-Methoxy-5-(1-methyl-1H-pyrazol-4-yl)pyridin-2-ylamine → N-(6-Methoxy-5-(1-methyl-1H-pyrazol-4-yl)pyridin-2-yl)-4-methyl-2-(4-methylthiazol-2-yl)-2,3,4,5-tetrahydropyrido[3,2-f][1,4]oxazepin-8-amine

https://huagongshe.com/reaction/311

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-Methoxy-5-(1-methyl-1H-pyrazol-4-yl)pyridin-2-ylamineHCID 57512866—
Reactant8-Chloro-4-methyl-2-(4-methylthiazol-2-yl)-2,3,4,5-tetrahydropyrido[3,2-f][1,4]oxazepineHCID 57512871—
ReagentCesium carbonateHCID 10796—
Catalyst2-(Dicyclohexylphosphino)biphenylHCID 2734216—
CatalystPalladium (II) acetateHCID 4144353—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductN-(6-Methoxy-5-(1-methyl-1H-pyrazol-4-yl)pyridin-2-yl)-4-methyl-2-(4-methylthiazol-2-yl)-2,3,4,5-tetrahydropyrido[3,2-f][1,4]oxazepin-8-amineHCID 5751282956.41%

Reaction Conditions

Temperature110 °C

Reaction Steps

To 8-chloro-4-methyl-2-(4-methylthiazol-2-yl)-2,3,4,5-tetrahydropyrido[3,2-f][1,4]oxazepine (207 mg, 0.70 mmol) in DME (3 mL) were 6-methoxy-5-(1-methyl-1H-pyrazol-4-yl)pyridin-2-amine (143 mg, 0.70 mmol), cesium carbonate (342 mg, 1.05 mmol), 2-(Dicyclohexylphosphino)biphenyl (24.53 mg, 0.07 mmol) and Palladium acetate (15.71 mg, 0.07 mmol) added. The reaction was heated to 110°C for 60 min under N2 atmosphere. The solids were filtered off and washed with DCM, the solvents were evaporated and the crude product was purified by silica flash chromatography using DCM : [DCM:MeOH:NH3 = 90:10:1] = 100:0 to 35:65 as gradient. The title compound was obtained as yellow foam.

Provenance & Evidence

Source dataset750 AstraZeneca ELN dataset
ORD IDord-980427b3cc854bc88aa11ec4ee256fb1
Source note750 AstraZeneca ELN dataset