HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2260832Generated: October 25, 2026
Acetic Acid → 9-methyl-3-[(2-methyl-1H-imidazol-1-yl)methyl]-1,2,3,9-tetrahydro-4H-carbazol-4-one glyoxylic acid
https://huagongshe.com/reaction/2260832
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Ondansetron | HCID 4595 | — |
| Reactant | Perchloric Acid | HCID 24247 | — |
| Product | 9-methyl-3-[(2-methyl-1H-imidazol-1-yl)methyl]-1,2,3,9-tetrahydro-4H-carbazol-4-one glyoxylic acid | HCID 86748675 | — |
Reaction Steps
A mixture containing 2.83 g (0.01 mole) of 3-hydroxy-methyl-9-methyl-1,2,3,9-tetrahydro-4H-carbazol-4-one-3-glyoxylic acid lactone [compound of the formula (Ic)]and 1.64 g (0.02 mole) of 2-methylimidazole in 6.0 ml of sulfolane (tetramethylenesulfone) is heated in an oil bath of 150 to 160° C. for 15 minutes while stirring. After cooling down and diluting with 60 ml of acetone the precipitate is filtered off, washed with acetone and dried to give 0.95 g of the title compound, m.p.: 190°-200° C. (with decomposition). The active agent content of this product measured by titration with perchloric acid in glacial acetic acid was found to be 96%. In the combined filtrate of the reaction, ondansetron could be detected by thin layer chromatography. The most important characteristics of the title product are as follows:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05478949 |
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| Source dataset | uspto-grants-1995_12 |
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| ORD ID | ord-e269cc799d2b4141a928ab8a459bf827 |
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| Source note | uspto-grants-1995_12 |
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