135197-44-3Relevant articles and documents
Process for the preparation of 9-deazaguanine derivatives
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Page 11, (2010/02/09)
Derivatives of 9-deazaguanine are prepared by reacting an aldehyde or ketone with a dialkylaminomalonate to form the corresponding enamine. The enamine is then reacted with a base to form a cyclic pyrrole. The cyclic pyrrole is reacted with an urea compound or a derivative of carbamimidoic acid to provide a protected guanidino compound. The guanidino is converted to the desired 9-deazaguanine derivative by reacting with trifluoracetic acid or with an alkoxide or hydroxide followed by neutralization with an acid.
Structure-based design of inhibitors of purine nucleoside phosphorylase. 2. 9-Alicyclic and 9-heteroalicyclic derivatives of 9-deazaguanine
Secrist III,Niwas,Rose,Babu,Bugg,Erion,Guida,Ealick,Montgomery
, p. 1847 - 1854 (2007/10/02)
Alicyclic and heteroalicyclic derivatives of 9-deazaguanine (2-amino-1,5- dihydro-4H-pyrrolo[3,2-d][pyrimidin-4-one) are, with one exception, potent inhibitors of purine nucleoside phosphorylase (PNP) equaling the corresponding 9-arylmethyl derivatives pr