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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantThionyl ChlorideHCID 24386—
Reactant6-Bromopyrazolo(1,5-a)pyridine-3-carboxylic acidHCID 57372319—
ReactantMethyl 5-amino-6-methylnicotinateHCID 58662456—
SolventTolueneHCID 1140—
ProductMethyl 5-(6-bromopyrazolo[1,5-a]pyridine-3-carboxamido)-6-methylnicotinateHCID 71282967—

Reaction Conditions

Temperature110 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09073921B2
Source datasetuspto-grants-2015_07
ORD IDord-53cceb0558e34c3489ef2261b591c60d
Source noteuspto-grants-2015_07