(2R)-2-[[9-isopropyl-6-[[4-[3-(methoxy)propoxy]benzyl]amino]-9H-purin-2-yl]amino]-butanol

Base Information

• Chemical Name: (2R)-2-[[9-isopropyl-6-[[4-[3-(methoxy)propoxy]benzyl]amino]-9H-purin-2-yl]amino]-butanol
• CAS No.: 1428320-04-0
• Molecular Formula: C₂₃H₃₄N₆O₃
• Molecular Weight: 442.561
• Mol file: 1428320-04-0.mol

Synonyms:(2R)-2-[[9-isopropyl-6-[[4-[3-(methoxy)propoxy]benzyl]amino]-9H-purin-2-yl]amino]-butanol

Chemical Property of (2R)-2-[[9-isopropyl-6-[[4-[3-(methoxy)propoxy]benzyl]amino]-9H-purin-2-yl]amino]-butanol

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of (2R)-2-[[9-isopropyl-6-[[4-[3-(methoxy)propoxy]benzyl]amino]-9H-purin-2-yl]amino]-butanol

There total 8 articles about (2R)-2-[[9-isopropyl-6-[[4-[3-(methoxy)propoxy]benzyl]amino]-9H-purin-2-yl]amino]-butanol 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: 42.0%

(2R)-2-[[6-benzylsulfonyl-9-isopropyl-9H-purin-2-yl]amino]-butanol (1428320-00-6) + 4-(3-methoxypropoxy)benzylamine (1094783-71-7) → (2R)-2-[[9-isopropyl-6-[[4-[3-(methoxy)propoxy]benzyl]amino]-9H-purin-2-yl]amino]-butanol (1428320-04-0)

Guidance literature:

With triethylamine; In ethanol; at 40 ℃; for 120h;

DOI:10.1016/j.bmc.2013.01.009

Reference yield:

6-chloro-2-iodo-(9H)-purine (18552-90-4) → (2R)-2-[[9-isopropyl-6-[[4-[3-(methoxy)propoxy]benzyl]amino]-9H-purin-2-yl]amino]-butanol (1428320-04-0)

Guidance literature:

Multi-step reaction with 5 steps

1: N-ethyl-N,N-diisopropylamine / ethanol / Reflux; Inert atmosphere

2: potassium carbonate / dimethyl sulfoxide / 50 °C

3: butan-1-ol / 120 h / Reflux

4: 3-chloro-benzenecarboperoxoic acid / dichloromethane / 3 h / 0 - 20 °C

5: triethylamine / ethanol / 120 h / 40 °C

With potassium carbonate; triethylamine; N-ethyl-N,N-diisopropylamine; 3-chloro-benzenecarboperoxoic acid; In ethanol; dichloromethane; dimethyl sulfoxide; butan-1-ol;

DOI:10.1016/j.bmc.2013.01.009

Reference yield:

(2R)-2-[(6-benzylsulfanyl-9-isopropylpurin-2-yl)amino]butan-1-ol (1428319-99-6) → (2R)-2-[[9-isopropyl-6-[[4-[3-(methoxy)propoxy]benzyl]amino]-9H-purin-2-yl]amino]-butanol (1428320-04-0)

Guidance literature:

Multi-step reaction with 2 steps

1: 3-chloro-benzenecarboperoxoic acid / dichloromethane / 3 h / 0 - 20 °C

2: triethylamine / ethanol / 120 h / 40 °C

With triethylamine; 3-chloro-benzenecarboperoxoic acid; In ethanol; dichloromethane;

DOI:10.1016/j.bmc.2013.01.009

upstream raw materials:

6-chloro-2-iodo-(9H)-purine

(2R)-2-[(6-benzylsulfanyl-9-isopropylpurin-2-yl)amino]butan-1-ol

(2R)-2-[[6-benzylsulfonyl-9-isopropyl-9H-purin-2-yl]amino]-butanol

4-(3-methoxypropoxy)benzylamine