5-iodo-7-Methyl-7H-pyrrolo[2,3-d]pyriMidin-4-aMine

Base Information

• Chemical Name: 5-iodo-7-Methyl-7H-pyrrolo[2,3-d]pyriMidin-4-aMine
• CAS No.: 862729-13-3
• Molecular Formula: C7H7IN4
• Molecular Weight: 274.064
• Mol file: 862729-13-3.mol

Synonyms:7H-Pyrrolo[2,3-d]pyrimidin-4-amine,5-iodo-7-methyl;5-iodo-7-methyl-7H-pyrrolo[2,3-d]pyrimidin-4-amine;5-iodo-7-methyl-7H-pyrrolo[2,3-d]pyrimidin-4-ylamine;

Chemical Property of 5-iodo-7-Methyl-7H-pyrrolo[2,3-d]pyriMidin-4-aMine

Chemical Property:

• PSA: 56.73000
• LogP: 1.73630
• Storage Temp.: 2-8°C(protect from light)

Purity/Quality:

99%, ^*data from raw suppliers

5-Iodo-7-methyl-7H-pyrrolo[2,3-d]pyrimidin-4-amine 95+% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

Technology Process of 5-iodo-7-Methyl-7H-pyrrolo[2,3-d]pyriMidin-4-aMine

There total 7 articles about 5-iodo-7-Methyl-7H-pyrrolo[2,3-d]pyriMidin-4-aMine 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: 50.0%

4-amino-5-iodo-7H-pyrrolo[2,3‐d]pyrimidine (163622-50-2) + methyl iodide (74-88-4) → 4-amino-5-iodo-7-methylpyrrolo[2,3‐d]pyrimidine (862729-13-3)

Guidance literature:

With potassium carbonate; In N,N-dimethyl-formamide; for 8h;

Reference yield:

Allopurinol (3680-71-5) → 4-amino-5-iodo-7-methylpyrrolo[2,3‐d]pyrimidine (862729-13-3)

Guidance literature:

Multi-step reaction with 4 steps

1: trichlorophosphate; triethylamine; N-ethyl-N,N-diisopropylamine / 3 h / 50 °C

2: ammonia / ethanol / 2 h / 60 °C

3: N-iodo-succinimide / dichloromethane / 13 h / 20 °C

4: caesium carbonate / 12 h / Reflux

With N-iodo-succinimide; ammonia; caesium carbonate; triethylamine; N-ethyl-N,N-diisopropylamine; trichlorophosphate; In ethanol; dichloromethane;

Reference yield:

4-chloro-5-iodo-7-methyl-7H-pyrrolo[2,3-d]pyrimidine (833481-37-1) → 4-amino-5-iodo-7-methylpyrrolo[2,3‐d]pyrimidine (862729-13-3)

Guidance literature:

With ammonia; In methanol; at 110 ℃;

upstream raw materials:

4-chloro-5-iodo-7-methyl-7H-pyrrolo[2,3-d]pyrimidine

4-amino-5-iodo-7H-pyrrolo[2,3‐d]pyrimidine

methyl iodide

7-deazaadenine

Downstream raw materials:

1,1-dimethylethyl 5-(4-amino-7-methyl-7H-pyrrolo[2,3-d]pyrimidin-5-yl)-2,3-dihydro-1H-indole-1-carboxylate

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