4-<<(dimethylamino)methylidene>amino>-7-<3-O-<(1,1-dimethylethyl)dimethylsilyl>-5-O-<(4-methoxytriphenyl)methyl>-β-D-ribofuranosyl>-7H-pyrrolo<2,3-d>pyrimidine

Base Information

• Chemical Name: 4-<<(dimethylamino)methylidene>amino>-7-<3-O-<(1,1-dimethylethyl)dimethylsilyl>-5-O-<(4-methoxytriphenyl)methyl>-β-D-ribofuranosyl>-7H-pyrrolo<2,3-d>pyrimidine
• CAS No.: 151512-09-3
• Molecular Formula: C₄₀H₄₉N₅O₅Si
• Molecular Weight: 707.945
• Mol file: 151512-09-3.mol

Synonyms:

Chemical Property of 4-<<(dimethylamino)methylidene>amino>-7-<3-O-<(1,1-dimethylethyl)dimethylsilyl>-5-O-<(4-methoxytriphenyl)methyl>-β-D-ribofuranosyl>-7H-pyrrolo<2,3-d>pyrimidine

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 4-<<(dimethylamino)methylidene>amino>-7-<3-O-<(1,1-dimethylethyl)dimethylsilyl>-5-O-<(4-methoxytriphenyl)methyl>-β-D-ribofuranosyl>-7H-pyrrolo<2,3-d>pyrimidine

There total 4 articles about 4-<<(dimethylamino)methylidene>amino>-7-<3-O-<(1,1-dimethylethyl)dimethylsilyl>-5-O-<(4-methoxytriphenyl)methyl>-β-D-ribofuranosyl>-7H-pyrrolo<2,3-d>pyrimidine which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 41.0%

tert-butyldimethylsilyl chloride (18162-48-6) + 4-<<(dimethylamino)methylidene>amino>-7-<5-O-<(4-methoxytriphenyl)methyl>-β-D-ribofuranosyl>-7H-pyrrolo<2,3-d>pyrimidine (57881-44-4) → 4-<<(dimethylamino)methylidene>amino>-7-<3-O-<(1,1-dimethylethyl)dimethylsilyl>-5-O-<(4-methoxytriphenyl)methyl>-β-D-ribofuranosyl>-7H-pyrrolo<2,3-d>pyrimidine (151512-09-3) + 4-<<(dimethylamino)methylidene>amino>-7-<2-O-<(1,1-dimethylethyl)dimethylsilyl>-5-O-<(4-methoxytriphenyl)methyl>-β-D-ribofuranosyl>-7H-pyrrolo<2,3-d>pyrimidine + 4-<<(dimethylamino)methylidene>amino>-7-<2,3-O-bis<(1,1-dimethylethyl)dimethylsilyl>-5-O-<(4-methoxytriphenyl)methyl>-β-D-ribofuranosyl>-7H-pyrrolo<2,3-d>pyrimidine

Guidance literature:

With 1H-imidazole; In pyridine; for 24h;

DOI:10.1002/hlca.19930760502

Reference yield: 17.0%

tert-butyldimethylsilyl chloride (18162-48-6) + 4-<<(dimethylamino)methylidene>amino>-7-<5-O-<(4-methoxytriphenyl)methyl>-β-D-ribofuranosyl>-7H-pyrrolo<2,3-d>pyrimidine (57881-44-4) → 4-<<(dimethylamino)methylidene>amino>-7-<3-O-<(1,1-dimethylethyl)dimethylsilyl>-5-O-<(4-methoxytriphenyl)methyl>-β-D-ribofuranosyl>-7H-pyrrolo<2,3-d>pyrimidine (151512-09-3) + 4-<<(dimethylamino)methylidene>amino>-7-<2-O-<(1,1-dimethylethyl)dimethylsilyl>-5-O-<(4-methoxytriphenyl)methyl>-β-D-ribofuranosyl>-7H-pyrrolo<2,3-d>pyrimidine

Guidance literature:

With silver nitrate; In tetrahydrofuran; pyridine; for 24h;

DOI:10.1002/hlca.19930760502

Reference yield:

tubercidin (69-33-0) → 4-<<(dimethylamino)methylidene>amino>-7-<3-O-<(1,1-dimethylethyl)dimethylsilyl>-5-O-<(4-methoxytriphenyl)methyl>-β-D-ribofuranosyl>-7H-pyrrolo<2,3-d>pyrimidine (151512-09-3)

Guidance literature:

Multi-step reaction with 3 steps

1: 85 percent / dimethylformamide / 1 h / 50 °C

2: 81 percent / (i-Pr)2NEt / pyridine / 3 h / 50 °C

3: 17 percent / AgNO₃ / pyridine; tetrahydrofuran / 24 h

With silver nitrate; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; pyridine; N,N-dimethyl-formamide;

DOI:10.1002/hlca.19930760502

upstream raw materials:

tert-butyldimethylsilyl chloride

4-<<(dimethylamino)methylidene>amino>-7-<5-O-<(4-methoxytriphenyl)methyl>-β-D-ribofuranosyl>-7H-pyrrolo<2,3-d>pyrimidine

tubercidin

4-<<(dimethylamino)methylidene>amino>-7-(β-D-ribofuranosyl)-7H-pyrrolo<2,3-d>pyrimidine