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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1931336Generated: November 3, 2026

Sodium Carbonate → HCID 57598028, compound

https://huagongshe.com/reaction/1931336

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant2-Chloropyridine-4-boronic acidHCID 5151595—
Reactant3-Bromo-1-(4-methylbenzene-1-sulfonyl)-1H-pyrrolo[2,3-b]pyridineHCID 21669155—
CatalystHCID 178418397HCID 178418397—
Solvent1,2-DimethoxyethaneHCID 8071—
SolventEthyl AcetateHCID 8857—
ProductHCID 57598028HCID 5759802868%

Reaction Steps

A mixture of azaindole 3 (80 mg, 0.23 mmol), 2-chloropyridine-4-boronic acid (41 mg, 0.27 mmol), Pd(Ph3P)4 (20 mg, 0.11 mmol) and 2 M sodium carbonate (0.34 mL, 0.68 mmol) in 2 mL of DME was microwaved on high at 160° C. for under nitrogen for 15 minutes. Diluted with ethyl acetate and the organic phase washed with water and brine then dried (Na2SO4) and concentrated in vacuo. The residue was subjected to flash chromatography (40% EtOAc/60% hexanes) to give 60 mg (68%) of the desired product 14. 1H NMR CDCl3 8.6 (d, 2H), 8.1 (m, 4H), 7.25 (m, 5H), 2.5 (s, 3H). The 2-chloropyridine could be displaced, for example, with benzylamine in a microwave reaction at 250° C. for 30 min followed by deprotection to give compound 15.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08188281B2
Source datasetuspto-grants-2012_05
ORD IDord-dd2a4a7f3b0948dbb676fa1f05c16967
Source noteuspto-grants-2012_05