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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2111795Generated: November 1, 2026

Trifluoroacetic acid → HCID 67011225, compound

https://huagongshe.com/reaction/2111795

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant3-PyridinecarboxaldehydeHCID 10371—
ReactantTriethylsilaneHCID 12052—
ReactantHCID 69067477HCID 69067477—
SolventDichloromethaneHCID 6344—
ProductHCID 67011225HCID 67011225—

Reaction Steps

A solution of 1-(3-aminophenyl)-N-(pyridin-3-ylmethyl)-1H-benzimidazole-5-carboxamide (prepared in Steps (a)-(d) of the procedure used for the synthesis of EXAMPLE I1, 70.2 mg, 0.205 mmol) and nicotinaldehyde (20 μL, 0.21 mmol) in DCM (1 mL) under N2 was treated with TFA (1 mL) and after 5 min was heated at reflux for 2 h. The cooled reaction mixture was then treated with Et3SiH (70 μL, 0.44 mmol) and the mixture re-heated to reflux for 19 h. After this time the solvents and excess reagents were removed by concentration in vacuo and the crude residue purified by column chromatography over silica gel eluting with 0.7-15% MeOH/DCM to provide the title compound; MS (ES+): m/z 435 [MH+]

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07521448B2
Source datasetuspto-grants-2009_04
ORD IDord-b7a5c43647ca4006aee1ec07ecbffe39
Source noteuspto-grants-2009_04