N⁴-(5-cyclopropyl-1H-pyrazol-3-yl)-N²-((1-tosyl-1H-indol-4-yl)methyl)pyrimidine-2,4-diamine

Base Information

• Chemical Name: N⁴-(5-cyclopropyl-1H-pyrazol-3-yl)-N²-((1-tosyl-1H-indol-4-yl)methyl)pyrimidine-2,4-diamine
• CAS No.: 1425932-87-1
• Molecular Formula: C₂₆H₂₅N₇O₂S
• Molecular Weight: 499.596
• Mol file: 1425932-87-1.mol

Synonyms:N⁴-(5-cyclopropyl-1H-pyrazol-3-yl)-N²-((1-tosyl-1H-indol-4-yl)methyl)pyrimidine-2,4-diamine

Chemical Property of N⁴-(5-cyclopropyl-1H-pyrazol-3-yl)-N²-((1-tosyl-1H-indol-4-yl)methyl)pyrimidine-2,4-diamine

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of N⁴-(5-cyclopropyl-1H-pyrazol-3-yl)-N²-((1-tosyl-1H-indol-4-yl)methyl)pyrimidine-2,4-diamine

There total 6 articles about N⁴-(5-cyclopropyl-1H-pyrazol-3-yl)-N²-((1-tosyl-1H-indol-4-yl)methyl)pyrimidine-2,4-diamine 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: 48.0%

2-chloro-N-(3-cyclopropyl-1H-pyrazol-5-yl)pyrimidin-4-amine (851435-00-2) + (1-tosyl-1H-indol-4-yl)methanamine (1145678-74-5) → N4-(5-cyclopropyl-1H-pyrazol-3-yl)-N2-((1-tosyl-1H-indol-4-yl)methyl)pyrimidine-2,4-diamine (1425932-87-1)

Guidance literature:

With N-ethyl-N,N-diisopropylamine; In isopropyl alcohol; at 120 ℃; Sealed tube;

Reference yield:

1-[(4-methyl-phenyl)-sulfonyl]-1H-indol-4-carboxaldehyde (79681-04-2) → N4-(5-cyclopropyl-1H-pyrazol-3-yl)-N2-((1-tosyl-1H-indol-4-yl)methyl)pyrimidine-2,4-diamine (1425932-87-1)

Guidance literature:

Multi-step reaction with 3 steps

1: pyridine; hydroxylamine hydrochloride / ethanol / 70 °C

2: zinc; ammonium chloride / ethanol / Reflux

3: N-ethyl-N,N-diisopropylamine / isopropyl alcohol / 120 °C / Sealed tube

With pyridine; hydroxylamine hydrochloride; ammonium chloride; N-ethyl-N,N-diisopropylamine; zinc; In ethanol; isopropyl alcohol;

Reference yield:

1-tosyl-1H-indole-4-carbaldehyde oxime (1425932-86-0) → N4-(5-cyclopropyl-1H-pyrazol-3-yl)-N2-((1-tosyl-1H-indol-4-yl)methyl)pyrimidine-2,4-diamine (1425932-87-1)

Guidance literature:

Multi-step reaction with 2 steps

1: zinc; ammonium chloride / ethanol / Reflux

2: N-ethyl-N,N-diisopropylamine / isopropyl alcohol / 120 °C / Sealed tube

With ammonium chloride; N-ethyl-N,N-diisopropylamine; zinc; In ethanol; isopropyl alcohol;

upstream raw materials:

p-toluenesulfonyl chloride

4-formyl indole

1-[(4-methyl-phenyl)-sulfonyl]-1H-indol-4-carboxaldehyde

1-tosyl-1H-indole-4-carbaldehyde oxime