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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 305Generated: October 25, 2026

4-(Trifluoromethyl)benzylamine → 6-[[4-(Trifluoromethyl)phenyl]methylamino]pyridine-3-carboxamide

https://huagongshe.com/reaction/305

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Trifluoromethyl)benzylamineHCID 76804—
Reactant6-ChloronicotinamideHCID 80456—
ReagentSodium t-butoxideHCID 23676156—
CatalystBinap, (A+-)-HCID 634876—
CatalystPalladium (II) acetateHCID 4144353—
Solvent1,2-DimethoxyethaneHCID 8071—
Product6-[[4-(Trifluoromethyl)phenyl]methylamino]pyridine-3-carboxamideHCID 789156507.4%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a stirred solution of 6-chloronicotinamide (0.053 g, 0.34 mmol), 2,2'-bis(diphenylphosphino)-1,1'-binaphthyl (0.021 g, 0.03 mmol), sodium 2-methylpropan-2-olate (0.065 g, 0.68 mmol) and diacetoxypalladium (7.60 mg, 0.03 mmol) in DME (1 mL) was added (4-(trifluoromethyl)phenyl)methanamine (0.097 mL, 0.68 mmol). The reaction was run in microwave at 100 °C for 4h. The compound was purified by preparative HPLC on a Kromasil C8 column (10 µm 250x20 ID mm) using a gradient of 51-55% acetonitrile in H2O/ACN/FA 95/5/0.2 buffer, over 25 minutes with a flow of 19 mL/min. The compounds were detected by UV at 270nm. 6-(4-(trifluoromethyl)benzylamino)nicotinamide (7.40 mg, 7.40 %) was obtained.

Provenance & Evidence

Source dataset750 AstraZeneca ELN dataset
ORD IDord-92bacb0740454b4398d7f3969518ce26
Source note750 AstraZeneca ELN dataset