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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Pyruvic Acid | HCID 1060 | — |
| Reactant | Dabco | HCID 9237 | — |
| Reactant | 2-Amino-5-chloro-3-iodopyridine | HCID 11076010 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5-chloro-1H-pyrrolo[2,3-b]pyridine-2-carboxylic acid | HCID 44630705 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07405210B2 |
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| Source dataset | uspto-grants-2008_07 |
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| ORD ID | ord-8d78a663551244498906c537eab88b65 |
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| Source note | uspto-grants-2008_07 |
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