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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Anzemet | HCID 3148 | — |
| Reactant | Methanesulfonic Acid | HCID 6395 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | methanesulfonic acid;(10-oxo-8-azatricyclo[5.3.1.03,8]undecan-5-yl) 1H-indole-3-carboxylate;hydrate | HCID 22058225 | 148.8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07745628B2 |
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| Source dataset | uspto-grants-2010_06 |
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| ORD ID | ord-7be6600dba3e4bbd9e8aa81eb57a4489 |
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| Source note | uspto-grants-2010_06 |
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