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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 437Generated: October 28, 2026

HCID 58464469, compound → (R)-N-(2-(tert-butyldimethylsilyloxy)propyl)-2',6'-difluorobiphenyl-4-amine

https://huagongshe.com/reaction/437

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 58464469HCID 58464469—
Reactant(R)-2-(tert-butyldimethylsilyloxy)propan-1-amineHCID 59302513—
ReagentCesium carbonateHCID 10796—
CatalystPalladium (II) acetateHCID 4144353—
Catalyst2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenylHCID 11155794—
SolventTolueneHCID 1140—
Product(R)-N-(2-(tert-butyldimethylsilyloxy)propyl)-2',6'-difluorobiphenyl-4-amineHCID 6743983259.39%

Reaction Conditions

Temperature120 °C

Reaction Steps

PdOAc2 (0.030 g, 0.13 mmol) and dicyclohexyl(2',4',6'-triisopropylbiphenyl-2-yl)phosphine (0.064 g, 0.13 mmol) were added in one portion to a degassed solution of 4'-bromo-2,6-difluorobiphenyl (0.36 g, 1.34 mmol), (R)-2-(tert- butyldimethylsilyloxy)propan-1-amine (0.355 g, 1.87 mmol) and cesium carbonate (0.654 g, 2.01 mmol) in toluene (10 mL) at 20°C under nitrogen. The resulting suspension was stirred at 120 °C for 50 hours. The reaction mixture was diluted with EtOAc (150 mL) and water (150 mL) and the biphasic mixture was filtered through celite. The organic layer was separated and washed sequentially with water (150 mL) and saturated brine (150 mL). The organic layer was evaporated to afford crude product. The crude product was purified by flash silica chromatography, elution gradient 0 to 10% EtOAc in isohexane. Pure fractions were evaporated to dryness to afford (R)-N-(2-(tert-butyldimethylsilyloxy)propyl)-2',6'-difluorobiphenyl-4-amine (0.300 g, 59.4 %) as a yellow solid.

Provenance & Evidence

Source dataset750 AstraZeneca ELN dataset
ORD IDord-c3293297b4c643b7b38f6be28fe8ecb0
Source note750 AstraZeneca ELN dataset