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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 494731Generated: October 31, 2026

Sodium Azide → HCID 86596995, compound

https://huagongshe.com/reaction/494731

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium AzideHCID 33557—
Reactant4,6-dichloro-5-methylnicotinic acidHCID 10726946—
ReactantHCID 21111553HCID 21111553—
ReactantHCID 58886666HCID 58886666—
ProductHCID 86596995HCID 86596995—

Reaction Conditions

Temperature50 °C

Reaction Steps

4,6-Dichloro-5-methylnicotinic acid (J. Heterocyclic Chemistry 1999, 36, 953-957) was converted to 7-(4-bromo-2-chloro-phenylamino)-8-methylimidazo[1,2-a]pyridine-6-carboxylic acid according to the steps described in the alternate synthesis of Step D, Example 9. It was determined that addition of sodium azide to the 4-(4-bromo-2-chloro-phenylamino)-6-chloro-5-methylnicotinic acid methyl ester intermediate required heating to 50° C., which results in a separable mixture of the desired methyl ester, 6-azido-4-(4-bromo-2-chlorophenylamino)-5-methylnicotinic acid methyl ester, and the corresponding carboxylic acid. MS ESI (+) m/z 380, 382 (M+, Cl, Br pattern) detected. 1H NMR (400 MHz, DMSO-d6) δ 9.46 (s, 1H), 9.40 (br s, 1H), 8.25 (d, 1H), 8.12 (d, 1H), 7.79 (m, 1H), 7.42 (dd, 1H), 6.80 (d, 1H), 2.07 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07538120B2
Source datasetuspto-grants-2009_05
ORD IDord-c236ef8ea6804f92a3383290ebe900a9
Source noteuspto-grants-2009_05