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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2373196Generated: October 30, 2026

Methanesulfonic Acid → Linaprazan mesylate

https://huagongshe.com/reaction/2373196

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonic AcidHCID 6395—
ReactantLinaprazanHCID 9951066—
SolventEthanolHCID 702—
ProductLinaprazan mesylateHCID 1124823280.8%

Reaction Conditions

Temperature60 °C

Reaction Steps

100 g of 2,3-dimethyl-8-(2,6-dimethylbenzylamino)-N-hydroxyethyl-imidazo[1,2-a]pyridine-6-carboxamide was suspended in 200 ml ethanol. The suspension was heated to approximately 60° C. and a mixture of methanesulphonic acid (28.9 g) and ethanol (40 ml) was charged during approximately 80 minutes. After rinsing with ethanol (10 ml), the suspension was cooled to approximately 50° C. The crystals were isolated and washed with ethanol. The crystals were dried (dry-blowing) during 1.5 h. 102 g of 2,3-dimethyl-8-(2,6-dimethylbenzylamino)-N-hydroxyethyl-imidazo[1,2-a]pyridine-6-carboxamide mesylate salt form A was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07459463B2
Source datasetuspto-grants-2008_12
ORD IDord-828781ec9e28476b92003dabe3008e2b
Source noteuspto-grants-2008_12