8-(4-METHOXYBENZYL)-5-METHYL-7,8-DIHYDRO-6H-PYRROLO[3,2-E][1,2,4]TRIAZOLO[1,5-A]PYRIMIDINE

Base Information

• Chemical Name: 8-(4-METHOXYBENZYL)-5-METHYL-7,8-DIHYDRO-6H-PYRROLO[3,2-E][1,2,4]TRIAZOLO[1,5-A]PYRIMIDINE
• CAS No.: 62052-77-1
• Molecular Formula: C₁₆H₁₇N₅O
• Molecular Weight: 295.344
• Mol file: 62052-77-1.mol

Synonyms:8-(4-methoxy-benzyl)-5-methyl-7,8-dihydro-6H-pyrrolo[3,2-e][1,2,4]triazolo[1,5-a]pyrimidine

Chemical Property of 8-(4-METHOXYBENZYL)-5-METHYL-7,8-DIHYDRO-6H-PYRROLO[3,2-E][1,2,4]TRIAZOLO[1,5-A]PYRIMIDINE

Chemical Property:

Purity/Quality:

METHYL-4-[(5-METHYL-6,7-DIHYDRO-8H-PYRROLO[3,2-E][1,2,4]TRIAZOLO[1,5-A]PYRIMIDIN-8-YL)METHYL]PHENYL ETHER 95.00% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 8-(4-METHOXYBENZYL)-5-METHYL-7,8-DIHYDRO-6H-PYRROLO[3,2-E][1,2,4]TRIAZOLO[1,5-A]PYRIMIDINE

There total 5 articles about 8-(4-METHOXYBENZYL)-5-METHYL-7,8-DIHYDRO-6H-PYRROLO[3,2-E][1,2,4]TRIAZOLO[1,5-A]PYRIMIDINE 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: 78.0%

7-chloro-6-(2-chloroethyl)-5-methyl-1,2,4-triazolo<1,5-a>pyrimidine (62053-05-8) + 4-methoxy-benzylamine (2393-23-9) → 8-(4-methoxy-benzyl)-5-methyl-7,8-dihydro-6H-pyrrolo[3,2-e][1,2,4]triazolo[1,5-a]pyrimidine (62052-77-1)

Guidance literature:

With sodium carbonate; In ethanol; for 2h; Heating;

DOI:10.1021/jm00182a021

Reference yield:

3-acetyl-2-oxo-4,5-dihydrofuran (517-23-7,594837-91-9,98634-97-0,313643-49-1) → 8-(4-methoxy-benzyl)-5-methyl-7,8-dihydro-6H-pyrrolo[3,2-e][1,2,4]triazolo[1,5-a]pyrimidine (62052-77-1)

Guidance literature:

Multi-step reaction with 4 steps

1: 88 percent / BF₃*MeOH / ethanol / 72 h / Ambient temperature

2: 89 percent / Et₃N / H₂O / 18 h / Ambient temperature

3: 78 percent / POCl₃ / 3 h / Heating

4: 78 percent / Na₂CO₃ / ethanol / 2 h / Heating

With boron trifluoride methanol complex; sodium carbonate; triethylamine; trichlorophosphate; In ethanol; water;

DOI:10.1021/jm00182a021

Reference yield:

6-(2-hydroxyethyl)-5-methyl-1,2,4-triazolo<1,5-a>pyrimidin-7(4H)-one (62053-06-9) → 8-(4-methoxy-benzyl)-5-methyl-7,8-dihydro-6H-pyrrolo[3,2-e][1,2,4]triazolo[1,5-a]pyrimidine (62052-77-1)

Guidance literature:

Multi-step reaction with 2 steps

1: 78 percent / POCl₃ / 3 h / Heating

2: 78 percent / Na₂CO₃ / ethanol / 2 h / Heating

With sodium carbonate; trichlorophosphate; In ethanol;

DOI:10.1021/jm00182a021

upstream raw materials:

7-chloro-6-(2-chloroethyl)-5-methyl-1,2,4-triazolo<1,5-a>pyrimidine

4-methoxy-benzylamine

3-acetyl-2-oxo-4,5-dihydrofuran

6-(2-hydroxyethyl)-5-methyl-1,2,4-triazolo<1,5-a>pyrimidin-7(4H)-one

Downstream raw materials:

8-(4-Methoxy-benzyl)-5-methyl-8H-pyrrolo[3,2-e][1,2,4]triazolo[1,5-a]pyrimidine

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