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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 20205Generated: October 29, 2026

Anzemet → methanesulfonic acid;(10-oxo-8-azatricyclo[5.3.1.03,8]undecan-5-yl) 1H-indole-3-carboxylate;hydrate

https://huagongshe.com/reaction/20205

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAnzemetHCID 3148—
ReactantMethanesulfonic AcidHCID 6395—
SolventAcetoneHCID 180—
Productmethanesulfonic acid;(10-oxo-8-azatricyclo[5.3.1.03,8]undecan-5-yl) 1H-indole-3-carboxylate;hydrateHCID 22058225148.8%

Reaction Conditions

Temperature25 °C

Reaction Steps

Methanesulphonic acid (0.34 mL, 5.24 mmol) is added to a solution of 1H-Indole-3-carboxylic acid 10-oxo-8-aza-tricyclo[5.3.1.03,8]undec-5-yl ester (1.6 gr, 4.93 mmol) in acetone (20 mL) and under nitrogen, maintaining the reaction temperature around 25° C. Following stirring at 0° C. for 3 h, and at room temperature for one night, the solid that forms is filtered and washed with acetone. The product formed is recrystallised from isopropanol-water (95:5 by weight), to obtain 1H-Indole-3-carboxylic acid 10-oxo-8-aza-tricyclo[5.3.1.03,8]undec-5-yl ester methanesulphonate monohydrate (1.71 gr, 79%) in the form of a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07745628B2
Source datasetuspto-grants-2010_06
ORD IDord-7be6600dba3e4bbd9e8aa81eb57a4489
Source noteuspto-grants-2010_06