HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Temozolomide → 5-Amino-N4-(1,1-dimethylethyl)-N1-methyl-1H-imidazole-1,4-dicarboxamide
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Temozolomide | HCID 5394 | — |
| Edukt | 2-Cyano-N-(1,1-dimethylethyl)-2-[(diphenylmethylene)amino]acetamide | HCID 11393010 | — |
| Edukt | 2-amino-2-cyano-N-(1,1-dimethylethyl)-acetamide hydrochloride | HCID 22015422 | — |
| Produkt | 5-Amino-N4-(1,1-dimethylethyl)-N1-methyl-1H-imidazole-1,4-dicarboxamide | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US07612202B2 |
| Quelldatensatz | uspto-grants-2009_11 |
| ORD ID | ord-30d9ac5cf4b84f348e83266310595dc2 |
| Quellennotiz | uspto-grants-2009_11 |