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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantOndansetronHCID 4595—
ReactantPerchloric AcidHCID 24247—
Product9-methyl-3-[(2-methyl-1H-imidazol-1-yl)methyl]-1,2,3,9-tetrahydro-4H-carbazol-4-one glyoxylic acidHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05478949
Source datasetuspto-grants-1995_12
ORD IDord-e269cc799d2b4141a928ab8a459bf827
Source noteuspto-grants-1995_12