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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 751637Generated: October 27, 2026

Pyruvic Acid → 5-chloro-1H-pyrrolo[2,3-b]pyridine-2-carboxylic acid

https://huagongshe.com/reaction/751637

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyruvic AcidHCID 1060—
ReactantDabcoHCID 9237—
Reactant2-Amino-5-chloro-3-iodopyridineHCID 11076010—
Catalystpalladium(II) acetateHCID 167845—
SolventDimethylformamideHCID 6228—
Product5-chloro-1H-pyrrolo[2,3-b]pyridine-2-carboxylic acidHCID 44630705—

Reaction Conditions

Temperature110 °C

Reaction Steps

Pyruvic acid (0.43 ml, 6.24 mmol) was added to a solution of 5-chloro-3-iodopyridin-2-ylamine (Preparation 56, 500 mg, 2.08 mmol), palladium acetate (23 mg, 0.10 mmol) and DABCO (700 mg, 6.24 mmol) in anhydrous DMF (20 ml). The reaction mixture was degassed with argon for 20 min, then heated to 110° C. for 16 h. The solvent was removed in vacuo and the residue suspended in water (10 ml) and acetic acid (5 ml) and then filtered. The solid was dissolved in EtOAc (50 ml), extracted into 2N NaOH solution (50 ml) and the organic layer discarded. The aqueous solution was acidified with concentrated HCl and extracted into EtOAc (2×40 ml). The combined organics were dried (MgSO4) and concentrated in vacuo to give the title compound as a beige solid. δH (CD3OD): 7.14 (1H, s), 8.14 (1H, d), 8.35 (1H, d).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07405210B2
Source datasetuspto-grants-2008_07
ORD IDord-8d78a663551244498906c537eab88b65
Source noteuspto-grants-2008_07