Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2260832생성일: 2026년 10월 26일
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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Acetic Acid | HCID 176 | — |
| 반응물 | Ondansetron | HCID 4595 | — |
| 반응물 | Perchloric Acid | HCID 24247 | — |
| 생성물 | 9-methyl-3-[(2-methyl-1H-imidazol-1-yl)methyl]-1,2,3,9-tetrahydro-4H-carbazol-4-one glyoxylic acid | HCID 86748675 | — |
반응 단계
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:
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05478949 |
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| 출처 데이터셋 | uspto-grants-1995_12 |
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| ORD ID | ord-e269cc799d2b4141a928ab8a459bf827 |
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| 출처 메모 | uspto-grants-1995_12 |
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