HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1521334Generated: October 26, 2026
Pyridine → Methyl 5-(6-bromopyrazolo[1,5-a]pyridine-3-carboxamido)-6-methylnicotinate
https://huagongshe.com/reaction/1521334
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 6-Bromopyrazolo(1,5-a)pyridine-3-carboxylic acid | HCID 57372319 | — |
| Reactant | Methyl 5-amino-6-methylnicotinate | HCID 58662456 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Methyl 5-(6-bromopyrazolo[1,5-a]pyridine-3-carboxamido)-6-methylnicotinate | HCID 71282967 | — |
Reaction Steps
6-Bromopyrazolo[1,5-a]pyridine-3-carboxylic acid (7.71 g, 32.0 mmol) in toluene (80 ml) was treated with thionyl chloride (18.67 ml, 256 mmol) and was heated to 110° C. for 6 hr. The solvent was removed in vacuo and the residue was treated with pyridine (80 ml), methyl 5-amino-6-methylnicotinate (4.25 g, 25.6 mmol) and oven dried molecular sieves. The reaction mixture was stirred at RT overnight and then treated with MeOH (250 ml). The resulting suspension was removed by filtration. The filtrate was triturated with methanol and the solid produced was isolated to afford the title compound;
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09073921B2 |
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| Source dataset | uspto-grants-2015_07 |
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| ORD ID | ord-53cceb0558e34c3489ef2261b591c60d |
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| Source note | uspto-grants-2015_07 |
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