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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 36774생성일: 2026년 10월 24일

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/ko/reaction/36774

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물OndansetronHCID 4595—
반응물Perchloric AcidHCID 24247—
생성물9-methyl-3-[(2-methyl-1H-imidazol-1-yl)methyl]-1,2,3,9-tetrahydro-4H-carbazol-4-one glyoxylic acidHCID 86748675—

반응 단계

A mixture containing 2.83 g (0.01 mole) of 3-hydroxymethyl-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:

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05416221
출처 데이터셋uspto-grants-1995_05
ORD IDord-f7f751de6dd749f4979689779e45d824
출처 메모uspto-grants-1995_05