[(S)-1-(5-benzyl-7-cyano-1,3-dimethyl-2,4-dioxo-2,3,4,5-tetrahydro-1H-pyrrolo[3,2-d]pyrimidin-6-yl)-piperidin-3-yl]-carbamic acid tert-butyl ester

Base Information

• Chemical Name: [(S)-1-(5-benzyl-7-cyano-1,3-dimethyl-2,4-dioxo-2,3,4,5-tetrahydro-1H-pyrrolo[3,2-d]pyrimidin-6-yl)-piperidin-3-yl]-carbamic acid tert-butyl ester
• CAS No.: 942586-49-4
• Molecular Formula: C₂₆H₃₂N₆O₄
• Molecular Weight: 492.578
• Mol file: 942586-49-4.mol

Synonyms:[(S)-1-(5-benzyl-7-cyano-1,3-dimethyl-2,4-dioxo-2,3,4,5-tetrahydro-1H-pyrrolo[3,2-d]pyrimidin-6-yl)-piperidin-3-yl]-carbamic acid tert-butyl ester

Chemical Property of [(S)-1-(5-benzyl-7-cyano-1,3-dimethyl-2,4-dioxo-2,3,4,5-tetrahydro-1H-pyrrolo[3,2-d]pyrimidin-6-yl)-piperidin-3-yl]-carbamic acid tert-butyl ester

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of [(S)-1-(5-benzyl-7-cyano-1,3-dimethyl-2,4-dioxo-2,3,4,5-tetrahydro-1H-pyrrolo[3,2-d]pyrimidin-6-yl)-piperidin-3-yl]-carbamic acid tert-butyl ester

There total 8 articles about [(S)-1-(5-benzyl-7-cyano-1,3-dimethyl-2,4-dioxo-2,3,4,5-tetrahydro-1H-pyrrolo[3,2-d]pyrimidin-6-yl)-piperidin-3-yl]-carbamic acid tert-butyl 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:

5-benzyl-6-bromo-1,3-dimethyl-2,4-dioxo-2,3,4,5-tetrahydro-1H-pyrrolo[3,2-d]pyrimidine-7-carbonitrile (942586-88-1) + tert-butyl (S)-piperidin-3-yl-carbamate (216854-23-8,172603-05-3) → [(S)-1-(5-benzyl-7-cyano-1,3-dimethyl-2,4-dioxo-2,3,4,5-tetrahydro-1H-pyrrolo[3,2-d]pyrimidin-6-yl)-piperidin-3-yl]-carbamic acid tert-butyl ester (942586-49-4)

Guidance literature:

In DMA; at 160 ℃; for 0.666667h; Microwave;

Reference yield:

methyl bromide (74-83-9) + C25H30N6O4 (1360540-01-7) → [(S)-1-(5-benzyl-7-cyano-1,3-dimethyl-2,4-dioxo-2,3,4,5-tetrahydro-1H-pyrrolo[3,2-d]pyrimidin-6-yl)-piperidin-3-yl]-carbamic acid tert-butyl ester (942586-49-4)

Guidance literature:

With potassium carbonate; In N,N-dimethyl-formamide; at 20 ℃; for 18h;

DOI:10.1016/j.bmcl.2011.11.054

Reference yield:

C15H14N4O2 → [(S)-1-(5-benzyl-7-cyano-1,3-dimethyl-2,4-dioxo-2,3,4,5-tetrahydro-1H-pyrrolo[3,2-d]pyrimidin-6-yl)-piperidin-3-yl]-carbamic acid tert-butyl ester (942586-49-4)

Guidance literature:

Multi-step reaction with 5 steps

1: bromine; acetic acid / 18 h / 45 °C

2: 4-methyl-morpholine / N,N-dimethyl acetamide / 0.33 h / 160 °C / Microwave irradiation

3: palladium 10% on activated carbon; ammonium formate / 0.5 h / 75 °C

4: N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 60 °C

5: potassium carbonate / N,N-dimethyl-formamide / 18 h / 20 °C

With 4-methyl-morpholine; palladium 10% on activated carbon; bromine; ammonium formate; potassium carbonate; acetic acid; N-ethyl-N,N-diisopropylamine; In N,N-dimethyl acetamide; N,N-dimethyl-formamide;

DOI:10.1016/j.bmcl.2011.11.054

upstream raw materials:

5-benzyl-6-bromo-1,3-dimethyl-2,4-dioxo-2,3,4,5-tetrahydro-1H-pyrrolo[3,2-d]pyrimidine-7-carbonitrile

tert-butyl (S)-piperidin-3-yl-carbamate

methyl bromide

C₂₅H₃₀N₆O₄