Acetic acid (2R,3R,4R,5R)-2-(6-benzoylamino-purin-9-yl)-4-benzyloxy-5-((R)-1,2-diacetoxy-ethyl)-tetrahydro-furan-3-yl ester

Base Information

Chemical Name:Acetic acid (2R,3R,4R,5R)-2-(6-benzoylamino-purin-9-yl)-4-benzyloxy-5-((R)-1,2-diacetoxy-ethyl)-tetrahydro-furan-3-yl ester
CAS No.:184229-60-5
Molecular Formula:C₃₁H₃₁N₅O₉
Molecular Weight:617.615
Hs Code.:

Synonyms:Acetic acid (2R,3R,4R,5R)-2-(6-benzoylamino-purin-9-yl)-4-benzyloxy-5-((R)-1,2-diacetoxy-ethyl)-tetrahydro-furan-3-yl ester

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Chemical Property of Acetic acid (2R,3R,4R,5R)-2-(6-benzoylamino-purin-9-yl)-4-benzyloxy-5-((R)-1,2-diacetoxy-ethyl)-tetrahydro-furan-3-yl ester

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Technology Process of Acetic acid (2R,3R,4R,5R)-2-(6-benzoylamino-purin-9-yl)-4-benzyloxy-5-((R)-1,2-diacetoxy-ethyl)-tetrahydro-furan-3-yl ester

There total 4 articles about Acetic acid (2R,3R,4R,5R)-2-(6-benzoylamino-purin-9-yl)-4-benzyloxy-5-((R)-1,2-diacetoxy-ethyl)-tetrahydro-furan-3-yl ester 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: 71.0%

: 18055-47-5
N-Benzoyl-N,9-bis(trimethylsilyl)adenin

: 184229-59-2
3-O-benzyl-1,2:5,6-tetra-O-acetyl-β-D-allofuranose

: 184229-60-5
Acetic acid (2R,3R,4R,5R)-2-(6-benzoylamino-purin-9-yl)-4-benzyloxy-5-((R)-1,2-diacetoxy-ethyl)-tetrahydro-furan-3-yl ester

Guidance literature:: With trimethylsilyl trifluoromethanesulfonate; In acetonitrile; at 55 ℃; for 12h;
DOI:10.1021/ja961788h

Reference yield:

: 14686-89-6
(1,2:5,6)-di-O-isopropylidene-D-gulose

: 184229-60-5
Acetic acid (2R,3R,4R,5R)-2-(6-benzoylamino-purin-9-yl)-4-benzyloxy-5-((R)-1,2-diacetoxy-ethyl)-tetrahydro-furan-3-yl ester

Guidance literature:: Multi-step reaction with 3 steps

1: sodium hydride / dimethylformamide / 1 h / Ambient temperature

2: acetic acid, p-toluenesulfonic acid monohydrate / 1 h / Heating

3: 71 percent / trimethylsilyl trifluoromethanesulfonate / acetonitrile / 12 h / 55 °C

With trimethylsilyl trifluoromethanesulfonate; sodium hydride; toluene-4-sulfonic acid; acetic acid; In N,N-dimethyl-formamide; acetonitrile;
DOI:10.1021/ja961788h

Reference yield:

: 22331-21-1
1,2:5,6-di-O-isopropylidene-3-O-benzyl-α-D-allofuranose

: 184229-60-5
Acetic acid (2R,3R,4R,5R)-2-(6-benzoylamino-purin-9-yl)-4-benzyloxy-5-((R)-1,2-diacetoxy-ethyl)-tetrahydro-furan-3-yl ester

Guidance literature:: Multi-step reaction with 2 steps

1: acetic acid, p-toluenesulfonic acid monohydrate / 1 h / Heating

2: 71 percent / trimethylsilyl trifluoromethanesulfonate / acetonitrile / 12 h / 55 °C

With trimethylsilyl trifluoromethanesulfonate; toluene-4-sulfonic acid; acetic acid; In acetonitrile;
DOI:10.1021/ja961788h