Acetic acid (2R,3S,5R)-2-(6-benzoylamino-purin-9-yl)-4-{(2-cyano-ethoxy)-[(2R,3R,4S,5R)-3,4-diacetoxy-5-(6-benzoylamino-purin-9-yl)-tetrahydro-furan-2-ylmethoxy]-phosphoryloxy}-5-hydroxymethyl-tetrahydro-furan-3-yl ester

Base Information

Chemical Name:Acetic acid (2R,3S,5R)-2-(6-benzoylamino-purin-9-yl)-4-{(2-cyano-ethoxy)-[(2R,3R,4S,5R)-3,4-diacetoxy-5-(6-benzoylamino-purin-9-yl)-tetrahydro-furan-2-ylmethoxy]-phosphoryloxy}-5-hydroxymethyl-tetrahydro-furan-3-yl ester
CAS No.:122591-43-9
Molecular Formula:C₄₃H₄₂N₁₁O₁₅P
Molecular Weight:983.845
Hs Code.:

Acetic acid (2R,3S,5R)-2-(6-benzoylamino-purin-9-yl)-4-{(2-cyano-ethoxy)-[(2R,3R,4S,5R)-3,4-diacetoxy-5-(6-benzoylamino-purin-9-yl)-tetrahydro-furan-2-ylmethoxy]-phosphoryloxy}-5-hydroxymethyl-tetrahydro-furan-3-yl ester

Synonyms:Acetic acid (2R,3S,5R)-2-(6-benzoylamino-purin-9-yl)-4-{(2-cyano-ethoxy)-[(2R,3R,4S,5R)-3,4-diacetoxy-5-(6-benzoylamino-purin-9-yl)-tetrahydro-furan-2-ylmethoxy]-phosphoryloxy}-5-hydroxymethyl-tetrahydro-furan-3-yl ester

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Chemical Property of Acetic acid (2R,3S,5R)-2-(6-benzoylamino-purin-9-yl)-4-{(2-cyano-ethoxy)-[(2R,3R,4S,5R)-3,4-diacetoxy-5-(6-benzoylamino-purin-9-yl)-tetrahydro-furan-2-ylmethoxy]-phosphoryloxy}-5-hydroxymethyl-tetrahydro-furan-3-yl ester

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Technology Process of Acetic acid (2R,3S,5R)-2-(6-benzoylamino-purin-9-yl)-4-{(2-cyano-ethoxy)-[(2R,3R,4S,5R)-3,4-diacetoxy-5-(6-benzoylamino-purin-9-yl)-tetrahydro-furan-2-ylmethoxy]-phosphoryloxy}-5-hydroxymethyl-tetrahydro-furan-3-yl ester

There total 4 articles about Acetic acid (2R,3S,5R)-2-(6-benzoylamino-purin-9-yl)-4-{(2-cyano-ethoxy)-[(2R,3R,4S,5R)-3,4-diacetoxy-5-(6-benzoylamino-purin-9-yl)-tetrahydro-furan-2-ylmethoxy]-phosphoryloxy}-5-hydroxymethyl-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: 80.0%

: 122591-42-8
Acetic acid (2R,3S,5R)-2-(6-benzoylamino-purin-9-yl)-4-{(2-cyano-ethoxy)-[(2R,3R,4S,5R)-3,4-diacetoxy-5-(6-benzoylamino-purin-9-yl)-tetrahydro-furan-2-ylmethoxy]-phosphoryloxy}-5-[(4-methoxy-phenyl)-diphenyl-methoxymethyl]-tetrahydro-furan-3-yl ester

: 122591-43-9
Acetic acid (2R,3S,5R)-2-(6-benzoylamino-purin-9-yl)-4-{(2-cyano-ethoxy)-[(2R,3R,4S,5R)-3,4-diacetoxy-5-(6-benzoylamino-purin-9-yl)-tetrahydro-furan-2-ylmethoxy]-phosphoryloxy}-5-hydroxymethyl-tetrahydro-furan-3-yl ester

Guidance literature:: With acetic acid; In tetrahydrofuran; at 90 ℃; for 0.25h; var. solid phase synthesis, add of Vydac TP silica gel;
DOI:10.1016/S0040-4039(00)95378-4

Reference yield: 74.0%

: 122591-42-8
C₆₃H₅₈N₁₁O₁₆P

: 122591-43-9
Acetic acid (2R,3S,4R,5R)-2-(6-benzoylamino-purin-9-yl)-4-{(2-cyano-ethoxy)-[(2R,3R,4S,5R)-3,4-diacetoxy-5-(6-benzoylamino-purin-9-yl)-tetrahydro-furan-2-ylmethoxy]-phosphoryloxy}-5-hydroxymethyl-tetrahydro-furan-3-yl ester

Guidance literature:: With acetic acid; at 90 ℃; for 0.25h;

Reference yield:

: Acetic acid (2R,3S,5R)-2-(6-benzoylamino-purin-9-yl)-4-{(2-cyano-ethoxy)-[(2R,3R,4S,5R)-3,4-diacetoxy-5-(6-benzoylamino-purin-9-yl)-tetrahydro-furan-2-ylmethoxy]-phosphanyloxy}-5-[(4-methoxy-phenyl)-diphenyl-methoxymethyl]-tetrahydro-furan-3-yl ester

: 122591-43-9
Acetic acid (2R,3S,5R)-2-(6-benzoylamino-purin-9-yl)-4-{(2-cyano-ethoxy)-[(2R,3R,4S,5R)-3,4-diacetoxy-5-(6-benzoylamino-purin-9-yl)-tetrahydro-furan-2-ylmethoxy]-phosphoryloxy}-5-hydroxymethyl-tetrahydro-furan-3-yl ester

Guidance literature:: Multi-step reaction with 2 steps

1: I₂,H₂O / tetrahydrofuran / 0.08 h / var. solid phase synthesis, add of Vydac TP silica gel

2: 80 percent / 80percent AcOH / tetrahydrofuran / 0.25 h / 90 °C / var. solid phase synthesis, add of Vydac TP silica gel

With water; iodine; acetic acid; In tetrahydrofuran;
DOI:10.1016/S0040-4039(00)95378-4