CAS 91713-47-2

4-Chloro-1-[2-deoxy-3,5-bis-O-(4-methylbenzoyl)-β-D-erythro-pentofuranosyl]-1H-pyrazolo[3,4-d]pyrimidine

Description:

4-Chloro-1-[2-deoxy-3,5-bis-O-(4-methylbenzoyl)-β-D-erythro-pentofuranosyl]-1H-pyrazolo[3,4-d]pyrimidine is a complex organic compound characterized by its unique structural features, including a pyrazolo[3,4-d]pyrimidine core and a modified sugar moiety. The presence of a chloro group and two 4-methylbenzoyl substituents on the sugar enhances its chemical reactivity and solubility properties. This compound is likely to exhibit biological activity due to its structural similarity to nucleosides, which may influence its interaction with biological targets such as enzymes or receptors. Its synthesis involves multiple steps, including the protection of hydroxyl groups on the sugar and the introduction of the pyrazolo-pyrimidine framework. The compound's molecular weight, solubility in various solvents, and stability under different conditions would be critical for its application in research or pharmaceutical development. Overall, this compound represents a significant interest in medicinal chemistry, particularly in the context of developing new therapeutic agents.

Formula: C₂₆H₂₃ClN₄O₅

InChI: InChI=1S/C26H23ClN4O5/c1-15-3-7-17(8-4-15)25(32)34-13-21-20(36-26(33)18-9-5-16(2)6-10-18)11-22(35-21)31-24-19(12-30-31)23(27)28-14-29-24/h3-10,12,14,20-22H,11,13H2,1-2H3/t20-,21+,22+/m0/s1

InChI key: InChIKey=CPTREUTUTMYCBI-BHDDXSALSA-N

SMILES: O(C(=O)C1=CC=C(C)C=C1)[C@H]2C[C@H](N3C=4C(C=N3)=C(Cl)N=CN4)O[C@@H]2COC(=O)C5=CC=C(C)C=C5

Synonyms:

• 4-Chloro-1-[2-deoxy-3,5-bis-O-(4-methylbenzoyl)-β-D-erythro-pentofuranosyl]-1H-pyrazolo[3,4-d]pyrimidine
• 1H-Pyrazolo[3,4-d]pyrimidine, 4-chloro-1-[2-deoxy-3,5-bis-O-(4-methylbenzoyl)-β-D-erythro-pentofuranosyl]-