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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1661627Generated: October 30, 2026

Potassium Phosphate, Tribasic → 5-(6-chloro-1H-indol-2-yl)-pyridine-3-carbaldehyde

https://huagongshe.com/reaction/1661627

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant5-Bromo-3-pyridinecarboxaldehydeHCID 2784734—
Reactant2-Dicyclohexylphosphino-2',6'-dimethoxybiphenylHCID 11269872—
Reactant1-Boc-6-chloroindole-2-boronic acidHCID 44119151—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
Product5-(6-chloro-1H-indol-2-yl)-pyridine-3-carbaldehydeHCID 58215712—

Reaction Conditions

Temperature85 °C

Reaction Steps

A flask is charged with N-(tert-butoxycarbonyl)-6-chloro-1H-indol-2-ylboronic acid (8.3 g, 28.1 mmol), 5-bromonicotinaldehyde (4.35 g, 23.4 mmol), K3PO4 (9.94 g, 46.8 mmol), s-Phos (0.480 g, 1.170 mmol) and Pd2(dba)3 (0.429 g, 0.468 mmol), and the flask is flushed with N2. Toluene (250 mL) is added, and the mixture is heated to 85° C. for 1.5 h. The mixture is cooled to room temperature. Ethyl acetate (250 mL) is added and the mixture is filtered through a pad of silica gel, which is washed with EtOAc. Silica gel is added to the combined filtrate, which is concentrated in vacuo. The residue is placed under high vacuum at 63° C. overnight, and after elution with ethyl acetate, 5-(6-chloro-1H-indol-2-yl)-pyridine-3-carbaldehyde is obtained. MS (ESI) m/z 257.0 and 258.9 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08030334B2
Source datasetuspto-grants-2011_10
ORD IDord-f735456569744ca48a0f197c9a7c41ab
Source noteuspto-grants-2011_10