HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 44021Generated: October 23, 2026
Hydrochloric Acid → 6-Iodo-2-phenylpyrazolo[1,5-a]pyridine-3-carboxylic acid
https://huagongshe.com/en/reaction/44021
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Methyl 6-iodo-2-phenylpyrazolo[1,5-a]pyridine-3-carboxylate | HCID 59233743 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Lithium Hydroxide | HCID 3939 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 6-Iodo-2-phenylpyrazolo[1,5-a]pyridine-3-carboxylic acid | HCID 59233771 | 85% |
Reaction Steps
Methyl-6-iodo-2-phenylpyrazolo[1,5-a]pyridine-3-carboxylate (250 mg, 0.661 mmol) was dissolve in aqueous LiOH(2N,1 mL), methanol (2 mL) and tetrahydrofuran (7 mL). This solution was stirred overnight at 45° C. After 24 hours, 2 mL 2M LiOH and 2 mL methanol were added. Heated at 55° C. overnight. The reaction was cooled on an ice water bath and aqueous hydrochloric acid (10 mL, 1N) was added dropwise until acidic by pH paper. Ethylacetate (200 mL) and water (40 mL) were added. The organic portion was extracted with brine (20 mL) and was dried over magnesium sulfate. The solvent was removed by rotory evaporation. The residue was place under vacuum overnight to give of a white solid (204 mg, 85%). 1H NMR (500 MHz, DMSO-D6) δ ppm 7.47 (m, 3H) 7.77 (m, 2H) 7.97 (d, J=9.46 Hz, 1H) 9.27 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08536338B2 |
|---|
| Source dataset | uspto-grants-2013_09 |
|---|
| ORD ID | ord-ebd467546d364a949bbc9bec91c6b6a0 |
|---|
| Source note | uspto-grants-2013_09 |
|---|