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diisopropyl (S)-N2-benzoyl-9-[3-hydroxy-2-(phosphonomethoxy)propyl]guanine

Base Information
  • Chemical Name:diisopropyl (S)-N2-benzoyl-9-[3-hydroxy-2-(phosphonomethoxy)propyl]guanine
  • CAS No.:1374997-61-1
  • Molecular Formula:C22H30N5O7P
  • Molecular Weight:507.483
  • Hs Code.:
diisopropyl (S)-N<sub>2</sub>-benzoyl-9-[3-hydroxy-2-(phosphonomethoxy)propyl]guanine

Synonyms:diisopropyl (S)-N2-benzoyl-9-[3-hydroxy-2-(phosphonomethoxy)propyl]guanine

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Chemical Property of diisopropyl (S)-N2-benzoyl-9-[3-hydroxy-2-(phosphonomethoxy)propyl]guanine
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Technology Process of diisopropyl (S)-N2-benzoyl-9-[3-hydroxy-2-(phosphonomethoxy)propyl]guanine

There total 1 articles about diisopropyl (S)-N2-benzoyl-9-[3-hydroxy-2-(phosphonomethoxy)propyl]guanine 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:
Guidance literature:
(R)-9-<2-<(diisopropylphosphono)methoxy>-3-hydroxypropyl>guanine; With pyridine; trimethylsilyl bromide; for 0.5h;
benzoyl chloride; at 20 ℃; for 2h;
With ammonia; In water; at 20 ℃; for 0.5h;
DOI:10.1016/j.tet.2012.03.066
Guidance literature:
With sodium hypochlorite; sodium chlorite; 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; In acetonitrile; at 20 ℃; for 24h; pH=6.7; aq. phosphate buffer;
DOI:10.1016/j.tet.2012.03.066
Guidance literature:
Multi-step reaction with 2 steps
1: sodium chlorite; sodium hypochlorite; 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical / acetonitrile / 24 h / 20 °C / pH 6.7 / aq. phosphate buffer
2: trimethylsilyl bromide / acetonitrile / 20 °C
With sodium hypochlorite; sodium chlorite; 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; trimethylsilyl bromide; In acetonitrile;
DOI:10.1016/j.tet.2012.03.066
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