2,5-dimethyl-1-(2-phenylthiazol-4-ylmethyl)-1H-pyrrole-3-carboxylic acid 4-aminomethyl-benzylamide

Base Information

• Chemical Name: 2,5-dimethyl-1-(2-phenylthiazol-4-ylmethyl)-1H-pyrrole-3-carboxylic acid 4-aminomethyl-benzylamide
• CAS No.: 1618646-51-7
• Molecular Formula: C₂₅H₂₆N₄OS
• Molecular Weight: 430.574
• Mol file: 1618646-51-7.mol

Synonyms:2,5-dimethyl-1-(2-phenylthiazol-4-ylmethyl)-1H-pyrrole-3-carboxylic acid 4-aminomethyl-benzylamide

Chemical Property of 2,5-dimethyl-1-(2-phenylthiazol-4-ylmethyl)-1H-pyrrole-3-carboxylic acid 4-aminomethyl-benzylamide

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 2,5-dimethyl-1-(2-phenylthiazol-4-ylmethyl)-1H-pyrrole-3-carboxylic acid 4-aminomethyl-benzylamide

There total 4 articles about 2,5-dimethyl-1-(2-phenylthiazol-4-ylmethyl)-1H-pyrrole-3-carboxylic acid 4-aminomethyl-benzylamide 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: 64.0%

[4-({[2,5-dimethyl-1-(2-phenylthiazol-4-ylmethyl)-1H-pyrrole-3-carbonyl]amino}methyl)-benzyl]carbamic acid tert-butyl ester (1618647-86-1) → 2,5-dimethyl-1-(2-phenylthiazol-4-ylmethyl)-1H-pyrrole-3-carboxylic acid 4-aminomethyl-benzylamide (1618646-51-7)

Guidance literature:

With hydrogenchloride; water; In 1,4-dioxane; methanol; at 20 ℃; for 3h; Inert atmosphere;

Reference yield:

2,5-dimethyl-1-(2-phenyl-thiazol-4-ylmethyl)-1H-pyrrole-3-carboxylic acid (1618647-85-0) → 2,5-dimethyl-1-(2-phenylthiazol-4-ylmethyl)-1H-pyrrole-3-carboxylic acid 4-aminomethyl-benzylamide (1618646-51-7)

Guidance literature:

Multi-step reaction with 2 steps

1: benzotriazol-1-ol; triethylamine / dichloromethane; N,N-dimethyl-formamide / 18 h / 0 - 20 °C / Inert atmosphere

2: water; hydrogenchloride / methanol; 1,4-dioxane / 3 h / 20 °C / Inert atmosphere

With hydrogenchloride; water; benzotriazol-1-ol; triethylamine; In 1,4-dioxane; methanol; dichloromethane; N,N-dimethyl-formamide;

Reference yield:

1-[(2-phenylthiazol-4-yl)methyl]-2,5-dimethyl-1H-pyrrole-3-carboxylic acid ethyl ester (1618647-84-9) → 2,5-dimethyl-1-(2-phenylthiazol-4-ylmethyl)-1H-pyrrole-3-carboxylic acid 4-aminomethyl-benzylamide (1618646-51-7)

Guidance literature:

Multi-step reaction with 3 steps

1: sodium hydroxide; water / ethanol / 72 h / 90 °C / Inert atmosphere

2: benzotriazol-1-ol; triethylamine / dichloromethane; N,N-dimethyl-formamide / 18 h / 0 - 20 °C / Inert atmosphere

3: water; hydrogenchloride / methanol; 1,4-dioxane / 3 h / 20 °C / Inert atmosphere

With hydrogenchloride; water; benzotriazol-1-ol; triethylamine; sodium hydroxide; In 1,4-dioxane; methanol; ethanol; dichloromethane; N,N-dimethyl-formamide;

upstream raw materials:

1-[(2-phenylthiazol-4-yl)methyl]-2,5-dimethyl-1H-pyrrole-3-carboxylic acid ethyl ester

2,5-dimethyl-1-(2-phenyl-thiazol-4-ylmethyl)-1H-pyrrole-3-carboxylic acid

[4-({[2,5-dimethyl-1-(2-phenylthiazol-4-ylmethyl)-1H-pyrrole-3-carbonyl]amino}methyl)-benzyl]carbamic acid tert-butyl ester

ethyl 2-acetyl-4-oxopentanoate