(4aS,6R,7R,7aR)-6-(6-Amino-purin-9-yl)-1-benzyl-7-hydroxy-hexahydro-furo[3,2-d][1,3]oxazin-2-one

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Chemical Name:(4aS,6R,7R,7aR)-6-(6-Amino-purin-9-yl)-1-benzyl-7-hydroxy-hexahydro-furo[3,2-d][1,3]oxazin-2-one
CAS No.:182126-75-6
Molecular Formula:C₁₈H₁₈N₆O₄
Molecular Weight:382.379
Hs Code.:

Synonyms:(4aS,6R,7R,7aR)-6-(6-Amino-purin-9-yl)-1-benzyl-7-hydroxy-hexahydro-furo[3,2-d][1,3]oxazin-2-one

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Chemical Property of (4aS,6R,7R,7aR)-6-(6-Amino-purin-9-yl)-1-benzyl-7-hydroxy-hexahydro-furo[3,2-d][1,3]oxazin-2-one

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Technology Process of (4aS,6R,7R,7aR)-6-(6-Amino-purin-9-yl)-1-benzyl-7-hydroxy-hexahydro-furo[3,2-d][1,3]oxazin-2-one

There total 3 articles about (4aS,6R,7R,7aR)-6-(6-Amino-purin-9-yl)-1-benzyl-7-hydroxy-hexahydro-furo[3,2-d][1,3]oxazin-2-one 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: 88.0%

: 182126-72-3
Benzyl-carbamic acid (1R,2R,4R,5R)-4-(6-amino-purin-9-yl)-3,6-dioxa-bicyclo[3.1.0]hex-2-ylmethyl ester

: 182126-75-6
(4aS,6R,7R,7aR)-6-(6-Amino-purin-9-yl)-1-benzyl-7-hydroxy-hexahydro-furo[3,2-d][1,3]oxazin-2-one

Guidance literature:: With sodium hydride; In N,N-dimethyl-formamide; at 100 - 110 ℃; for 0.166667h;
DOI:10.1021/jo9606259

Reference yield:

: 2627-64-7
9-(2,3-anhydro-β-D-ribofuranosyl)adenine

: 182126-75-6
(4aS,6R,7R,7aR)-6-(6-Amino-purin-9-yl)-1-benzyl-7-hydroxy-hexahydro-furo[3,2-d][1,3]oxazin-2-one

Guidance literature:: Multi-step reaction with 2 steps

1: 1.) lipase from C_. antarctica, THF, 60 deg C, 24 h, 2.) THF, reflux, 8 h

2: 88 percent / NaH / dimethylformamide / 0.17 h / 100 - 110 °C

With sodium hydride; In N,N-dimethyl-formamide;
DOI:10.1021/jo9606259

Reference yield:

: 58-61-7
adenosine

: 182126-75-6
(4aS,6R,7R,7aR)-6-(6-Amino-purin-9-yl)-1-benzyl-7-hydroxy-hexahydro-furo[3,2-d][1,3]oxazin-2-one

Guidance literature:: Multi-step reaction with 3 steps

1: 1.) Me₂C(OAc)COBr, 2.) Dowex(OH-) / 1.) MeCN, H₂O, 2.) MeOH

2: 1.) lipase from C_. antarctica, THF, 60 deg C, 24 h, 2.) THF, reflux, 8 h

3: 88 percent / NaH / dimethylformamide / 0.17 h / 100 - 110 °C

With Dowex(OH-); acetoxyisobutyryl bromide; sodium hydride; In N,N-dimethyl-formamide;
DOI:10.1021/jo9606259