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HRID 16933作成日:2026年10月25日

Methyl Isocyanate → Temozolomide

https://huagongshe.com/reaction/16933

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl IsocyanateHCID 12228—
反応物4-amino-1H-imidazole-2-carboxamideHCID 21983288—
反応物5-diazo-1H-imidazole-4-carboxamideHCID 136377446—
溶媒DichloromethaneHCID 6344—
生成物TemozolomideHCID 5394—

反応手順

In this process, 5-amino-1H-imidazole-carboxamide (A) is converted into 5-diazo-1H-imidazole-4-carboxamide (B), which is then cyclized with methylisocyanate in dichloromethane to provide a high yield of clinical-grade Temozolomide. However, this process requires isolation of the unstable and potentially dangerous 5-diazo-1H-imidazole-4-carboxamide (B). Moreover, methylisocyanate is a difficult reagent to handle and ship, especially on the industrial scale, and indeed is better avoided in industrial manufacture. Furthermore, the cycloaddition of methylisocyanate requires a very long reaction time: Table I in J. Med. Chem. 1984, 27, 196-201, suggests 20 days.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07737284B2
出典データセットuspto-grants-2010_06
ORD IDord-d39ed1e4e8d04f3592ef23528a553348
出典メモuspto-grants-2010_06