(2S,3R)-2-[({4-amino-5-[(benzyloxy)methyl]-5H-pyrrolo[3,2-d]pyrimidin-7-yl}methyl)amino]-4-(methylsulfanyl)butane-1,3-diol

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Chemical Name:(2S,3R)-2-[({4-amino-5-[(benzyloxy)methyl]-5H-pyrrolo[3,2-d]pyrimidin-7-yl}methyl)amino]-4-(methylsulfanyl)butane-1,3-diol
CAS No.:1010824-10-8
Molecular Formula:C₂₀H₂₇N₅O₃S
Molecular Weight:417.532
Hs Code.:

Synonyms:(2S,3R)-2-[({4-amino-5-[(benzyloxy)methyl]-5H-pyrrolo[3,2-d]pyrimidin-7-yl}methyl)amino]-4-(methylsulfanyl)butane-1,3-diol

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Chemical Property of (2S,3R)-2-[({4-amino-5-[(benzyloxy)methyl]-5H-pyrrolo[3,2-d]pyrimidin-7-yl}methyl)amino]-4-(methylsulfanyl)butane-1,3-diol

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Technology Process of (2S,3R)-2-[({4-amino-5-[(benzyloxy)methyl]-5H-pyrrolo[3,2-d]pyrimidin-7-yl}methyl)amino]-4-(methylsulfanyl)butane-1,3-diol

There total 6 articles about (2S,3R)-2-[({4-amino-5-[(benzyloxy)methyl]-5H-pyrrolo[3,2-d]pyrimidin-7-yl}methyl)amino]-4-(methylsulfanyl)butane-1,3-diol 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:

: 1010824-09-5
(2S,3R)-2-[({5-[(benzyloxy)methyl]-4-chloro-5H-pyrrolo[3,2-d]pyrimidin-7-yl}methyl)amino]-4-(methylsulfanyl)butane-1,3-diol

: 1010824-10-8
(2S,3R)-2-[({4-amino-5-[(benzyloxy)methyl]-5H-pyrrolo[3,2-d]pyrimidin-7-yl}methyl)amino]-4-(methylsulfanyl)butane-1,3-diol

Guidance literature:: With ammonia; In methanol; at 135 ℃; for 24h; Sealed tube;
DOI:10.1016/j.bmc.2012.07.006

Reference yield:

: 1010701-76-4
5-[(benzyloxy)methyl]-7-bromo-4-chloro-5H-pyrrolo[3,2-d]pyrimidine

: 1010824-10-8
(2S,3R)-2-[({4-amino-5-[(benzyloxy)methyl]-5H-pyrrolo[3,2-d]pyrimidin-7-yl}methyl)amino]-4-(methylsulfanyl)butane-1,3-diol

Guidance literature:: Multi-step reaction with 3 steps

1.1: n-butyllithium / hexane; diethyl ether / -78 °C

1.2: -78 - -40 °C

2.1: sodium cyanoborohydride; acetyl chloride / methanol / 3 h / 20 °C

3.1: ammonia / methanol / 24 h / 135 °C / Sealed tube

With n-butyllithium; ammonia; sodium cyanoborohydride; acetyl chloride; In methanol; diethyl ether; hexane;
DOI:10.1016/j.bmc.2012.07.006

Reference yield:

: 1010701-75-3
5-[(benzyloxy)methyl]-4-chloro-5H-pyrrolo[3,2-d]pyrimidine-7-carbaldehyde

: 1010824-10-8
(2S,3R)-2-[({4-amino-5-[(benzyloxy)methyl]-5H-pyrrolo[3,2-d]pyrimidin-7-yl}methyl)amino]-4-(methylsulfanyl)butane-1,3-diol

Guidance literature:: Multi-step reaction with 2 steps

1: sodium cyanoborohydride; acetyl chloride / methanol / 3 h / 20 °C

2: ammonia / methanol / 24 h / 135 °C / Sealed tube

With ammonia; sodium cyanoborohydride; acetyl chloride; In methanol;
DOI:10.1016/j.bmc.2012.07.006