1998
DOI: 10.1002/chin.199839183
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ChemInform Abstract: Antitumor Imidazotetrazines. Part 36. Conversion of 5‐Aminoimidazole‐4‐carboxamide to Imidazo[5,1‐d][1,2,3,5]tetrazin‐4(3H)‐ones and Imidazo[1,5‐a][1,3,5]triazin‐4(3H)‐ones Related in Structure to the Antitumor Agents Temozolomide and Mitozolomide.

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“…Acid 6 was transformed into chloroanhydride 7 by the treatment with PCl 5 according to [23] that is a modified method reported in [24]. Previously, 3,3,3-trifluoroisocyanate 8 was synthesized from 3,3,3-trifluoroethylamine and phosgene [25–27], by thermal degradation of N -diphenyl- N '-(3,3,3-trifluoroethyl) urea [28, 29]. It was also synthesized using a Curtius reaction of chloroanhydride 7 and sodium azide [30], but isocyanate 8 was not isolated.…”
Section: Resultsmentioning
confidence: 99%
“…Acid 6 was transformed into chloroanhydride 7 by the treatment with PCl 5 according to [23] that is a modified method reported in [24]. Previously, 3,3,3-trifluoroisocyanate 8 was synthesized from 3,3,3-trifluoroethylamine and phosgene [25–27], by thermal degradation of N -diphenyl- N '-(3,3,3-trifluoroethyl) urea [28, 29]. It was also synthesized using a Curtius reaction of chloroanhydride 7 and sodium azide [30], but isocyanate 8 was not isolated.…”
Section: Resultsmentioning
confidence: 99%