HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1045410Generated: October 27, 2026
Hydrochloric Acid → 6-(3-Cyanopropyl)imidazo[1,2-a]pyridine-3-carboxylic acid
https://huagongshe.com/reaction/1045410
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | Ethyl 6-(3-cyanopropyl)imidazo[1,2-a]pyridine-3-carboxylate | HCID 71280341 | — |
| Solvent | MeOH tetrahydrofuran | HCID 21899815 | — |
| Product | 6-(3-Cyanopropyl)imidazo[1,2-a]pyridine-3-carboxylic acid | HCID 71280334 | — |
Reaction Steps
To a stirring solution of ethyl 6-(3-cyanopropyl)imidazo[1,2-a]pyridine-3-carboxylate (24w) (375 mg, 1.46 mmol) in THF:MeOH (4:1, 5 mL) was added 2N LiOH (500 μL). The reaction was heated at 50° C. for 45 minutes then cooled to room temperature and the pH was adjusted between 3-4 with 1N HCl. The solvent was partially concentrated and the remaining aqueous was lyophilized to yield 6-(3-cyanopropyl)imidazo[1,2-a]pyridine-3-carboxylic acid (25). 1H NMR (400 MHz, d6-DMSO) δ 9.21-9.19 (m, 1H), 8.45 (s, 1H), 7.85 (dd, J=0.8, 9.2 Hz, 1H), 7.70 (dd, J=1.6, 9.2 Hz, 1H), 2.82 (t, J=7.2 Hz, 2H), 2.55 (t, J=7.2 Hz, 2H), 1.97-1.90 (m, 2H). MS m/z 230.3 (M+1)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08569283B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-ab7c3b44c4034f83aa4f24ef06af25d8 |
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| Source note | uspto-grants-2013_10 |
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