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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1600173Generated: November 1, 2026

3-Pyridinecarboxaldehyde → HCID 10881145, compound

https://huagongshe.com/reaction/1600173

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-PyridinecarboxaldehydeHCID 10371—
ReactantTriethylsilaneHCID 12052—
Reactant5-Bromo-2-methylindoleHCID 5003968—
SolventDichloromethaneHCID 6344—
SolventTrifluoroacetic acidHCID 6422—
ProductHCID 10881145HCID 1088114575%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 5-bromo-2-methyl-1H-indole (J. Chem. Soc., 1428 (1965)) (2.0 g) and 3-pyridinecarboxaldehyde (1.02 g) in dry dichloromethane (20 ml) was added dropwise over 10 minutes to a stirred solution of triethylsilane(3.30 g) in trifluoroacetic acid (20 ml) at 0° C. The solution was stirred at 0° C. for 30 minutes and then evaporated under vacuum, keeping the temperature below 35° C. The residue was dissolved in dichloromethane, and the solution was washed with 2N sodium hydroxide, water and dried (MgSO4). The solution was evaporated and the residue was chromatographed on silica gel, using dichloromethane/methanol (50:1) as eluent. The product fractions were combined and evaporated, and the residue was crystallised from ether to give the title compound (2.15 g), m.p. 188°-190° C. Found: C,59.62; H,4.43; N,9.26. C15 H13BrN2 requires: C,59.82; H,4.35; N,9.30%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05744488
Source datasetuspto-grants-1998_04
ORD IDord-75f2916e50af49b79d8f15e75eef7ee4
Source noteuspto-grants-1998_04