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HRID 1433125Erstellt: 26. Oktober 2026

Temozolomide → 5-Amino-N4-(1,1-dimethylethyl)-N1-methyl-1H-imidazole-1,4-dicarboxamide

https://huagongshe.com/reaction/1433125

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTemozolomideHCID 5394—
Edukt2-Cyano-N-(1,1-dimethylethyl)-2-[(diphenylmethylene)amino]acetamideHCID 11393010—
Edukt2-amino-2-cyano-N-(1,1-dimethylethyl)-acetamide hydrochlorideHCID 22015422—
Produkt5-Amino-N4-(1,1-dimethylethyl)-N1-methyl-1H-imidazole-1,4-dicarboxamideHCID 11253427—

Reaktionsschritte

Another process for preparing Temozolomide is described in U.S. patent application having the Publication No. 2002/0095036 (see Scheme 4 below). In this process, the imine (V) is converted to 2-cyano-N-(1,1-dimethylethyl)-2-[(diphenyl-methylene)amino]-acetamide, which is converted to 2-amino-2-cyano-N-(1,1-dimethyl-ethyl)-acetamide hydrochloride. The latter is reacted with compound (VI) to obtain 5-amino-N4-(1,1-dimethylethyl)-N1-methyl-1H-imidazole-1,4-dicarboxamide, which is converted to 3,4-dihydro-N-(1,1-dimethylethyl)-3-methyl-imidazo-[5,1-d]-1,2,3,5-tetrazine-8-carboxamide (tert-butyl-Temozolomide), which yields Temozolomide under acidic treatment with concentrated sulfuric acid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07612202B2
Quelldatensatzuspto-grants-2009_11
ORD IDord-30d9ac5cf4b84f348e83266310595dc2
Quellennotizuspto-grants-2009_11