2-tert-butoxycarbonylamino-6-bromo-9-(2,4,5-tri-O-benzoyl-α-L-arabinofuranosyl)purine

Base Information

Chemical Name:2-tert-butoxycarbonylamino-6-bromo-9-(2,4,5-tri-O-benzoyl-α-L-arabinofuranosyl)purine
CAS No.:1311109-61-1
Molecular Formula:C₃₆H₃₂BrN₅O₉
Molecular Weight:758.582
Hs Code.:

Synonyms:2-tert-butoxycarbonylamino-6-bromo-9-(2,4,5-tri-O-benzoyl-α-L-arabinofuranosyl)purine

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Chemical Property of 2-tert-butoxycarbonylamino-6-bromo-9-(2,4,5-tri-O-benzoyl-α-L-arabinofuranosyl)purine

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Technology Process of 2-tert-butoxycarbonylamino-6-bromo-9-(2,4,5-tri-O-benzoyl-α-L-arabinofuranosyl)purine

There total 3 articles about 2-tert-butoxycarbonylamino-6-bromo-9-(2,4,5-tri-O-benzoyl-α-L-arabinofuranosyl)purine 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: 90.0%

: 1311109-74-6
N⁽²⁾-Boc-6-Br-2-aminopurine

: 1311109-69-9
2,3,5-tri-O-benzoyl-α-L-arabinofuranosyl ortho-hexynylbenzoate

: 1311109-61-1
2-tert-butoxycarbonylamino-6-bromo-9-(2,4,5-tri-O-benzoyl-α-L-arabinofuranosyl)purine

Guidance literature:: With [bis(trifluoromethanesulfonyl)imidate](triphenylphosphine)gold(I); In dichloromethane; at 20 ℃; Molecular sieve; Inert atmosphere;
DOI:10.1002/anie.201100514

Reference yield:

: 2,3,5-tri-O-benzoyl-α,β-L-arabinofuranose

: 1311109-61-1
2-tert-butoxycarbonylamino-6-bromo-9-(2,4,5-tri-O-benzoyl-α-L-arabinofuranosyl)purine

Guidance literature:: Multi-step reaction with 2 steps

1: dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine / dichloromethane / 3 h / 20 °C

2: [bis(trifluoromethanesulfonyl)imidate](triphenylphosphine)gold(I) / dichloromethane / 20 °C / Molecular sieve; Inert atmosphere

With dmap; [bis(trifluoromethanesulfonyl)imidate](triphenylphosphine)gold(I); 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; In dichloromethane;
DOI:10.1002/anie.201100514

Reference yield:

: 1311109-73-5
tris-Boc-6-Br-2-aminopurine

: 1311109-61-1
2-tert-butoxycarbonylamino-6-bromo-9-(2,4,5-tri-O-benzoyl-α-L-arabinofuranosyl)purine

Guidance literature:: Multi-step reaction with 2 steps

1: water; sodium hydroxide / ethanol / 80 h / 20 °C

2: [bis(trifluoromethanesulfonyl)imidate](triphenylphosphine)gold(I) / dichloromethane / 20 °C / Molecular sieve; Inert atmosphere

With [bis(trifluoromethanesulfonyl)imidate](triphenylphosphine)gold(I); water; sodium hydroxide; In ethanol; dichloromethane;
DOI:10.1002/anie.201100514