The nitroso group at the 5-position serves as a reactive functional group that can undergo reduction or further transformation to form key amine or coupling intermediates. This enables subsequent condensation with substituted cinnamic acid derivatives and facilitates ring modification and chain attachment, ultimately contributing to the construction of the substituted pyrimidine framework required for the final drug molecule. 6-Amino-1,3-diethyl-5-nitroso-2,4(1H,3H)-pyrimidinedione is an important intermediate derived from 5,6-diamino-1,3-diethyluracil in the synthesis of Istradefylline.
6-Amino-1,3-diethyl-5-nitroso-2,4(1H,3H)-pyrimidinedione
| API Name | Istradefylline |
|---|---|
| CAS No | 89073-60-9 |
| Molecular Formula | C8H12N4O3 |
| Molecular Weight | 212.21 g/mol |
| Synonyms | 6-amino-1,3-diethyl-5-nitrosopyrimidine-2,4-dione |
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Frequently Asked Questions
The nitroso group at the 5-position serves as a reactive functional group that can undergo reduction or further transformation to form key amine or coupling intermediates. This enables subsequent condensation with substituted cinnamic acid derivatives and facilitates ring modification and chain attachment, ultimately contributing to the construction of the substituted pyrimidine framework required for the final drug molecule. 6-Amino-1,3-diethyl-5-nitroso-2,4(1H,3H)-pyrimidinedione is an important intermediate derived from 5,6-diamino-1,3-diethyluracil in the synthesis of Istradefylline.
The CAS number of 6-Amino-1,3-diethyl-5-nitroso-2,4(1H,3H)-pyrimidinedione is 89073-60-9.
The molecular formula of 6-Amino-1,3-diethyl-5-nitroso-2,4(1H,3H)-pyrimidinedione is C8H12N4O3.
The listed molecular weight of 6-Amino-1,3-diethyl-5-nitroso-2,4(1H,3H)-pyrimidinedione is 212.21 g/mol.
6-Amino-1,3-diethyl-5-nitroso-2,4(1H,3H)-pyrimidinedione is listed as being used in connection with the following API: Istradefylline.
The listed synonym or IUPAC name for 6-Amino-1,3-diethyl-5-nitroso-2,4(1H,3H)-pyrimidinedione is 6-amino-1,3-diethyl-5-nitrosopyrimidine-2,4-dione.