[4-({1-Methyl-4-[(1-methyl-4-nitro-1H-pyrrole-2-carbonyl)-amino]-1H-pyrrole-2-carbonyl}-amino)-phenyl]-carbamic acid tert-butyl ester

Base Information

• Chemical Name: [4-({1-Methyl-4-[(1-methyl-4-nitro-1H-pyrrole-2-carbonyl)-amino]-1H-pyrrole-2-carbonyl}-amino)-phenyl]-carbamic acid tert-butyl ester
• CAS No.: 197705-52-5
• Molecular Formula: C₂₃H₂₆N₆O₆
• Molecular Weight: 482.496
• Mol file: 197705-52-5.mol

Synonyms:[4-({1-Methyl-4-[(1-methyl-4-nitro-1H-pyrrole-2-carbonyl)-amino]-1H-pyrrole-2-carbonyl}-amino)-phenyl]-carbamic acid tert-butyl ester

Chemical Property of [4-({1-Methyl-4-[(1-methyl-4-nitro-1H-pyrrole-2-carbonyl)-amino]-1H-pyrrole-2-carbonyl}-amino)-phenyl]-carbamic acid tert-butyl ester

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of [4-({1-Methyl-4-[(1-methyl-4-nitro-1H-pyrrole-2-carbonyl)-amino]-1H-pyrrole-2-carbonyl}-amino)-phenyl]-carbamic acid tert-butyl ester

There total 3 articles about [4-({1-Methyl-4-[(1-methyl-4-nitro-1H-pyrrole-2-carbonyl)-amino]-1H-pyrrole-2-carbonyl}-amino)-phenyl]-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:

1-methyl-4-nitro-pyrrol-2-carboxylic acid (13138-78-8) → [4-({1-Methyl-4-[(1-methyl-4-nitro-1H-pyrrole-2-carbonyl)-amino]-1H-pyrrole-2-carbonyl}-amino)-phenyl]-carbamic acid tert-butyl ester (197705-52-5)

Guidance literature:

Multi-step reaction with 4 steps

1: thionyl chloride / 0.67 h / Heating

2: 100 percent / pyridine / CH₂Cl₂ / 3 h / Ambient temperature

3: H₂ / 5percent Pd/C / methanol / 6 h / 760 Torr / Ambient temperature

4: pyridine / CH₂Cl₂ / 3 h / Ambient temperature

With pyridine; thionyl chloride; hydrogen; palladium on activated charcoal; In methanol; dichloromethane;

DOI:10.1016/S0968-0896(97)00096-5

Reference yield:

1-methyl-4-nitro-1H-pyrrole-2-carbonyl chloride (28494-51-1) → [4-({1-Methyl-4-[(1-methyl-4-nitro-1H-pyrrole-2-carbonyl)-amino]-1H-pyrrole-2-carbonyl}-amino)-phenyl]-carbamic acid tert-butyl ester (197705-52-5)

Guidance literature:

Multi-step reaction with 3 steps

1: 100 percent / pyridine / CH₂Cl₂ / 3 h / Ambient temperature

2: H₂ / 5percent Pd/C / methanol / 6 h / 760 Torr / Ambient temperature

3: pyridine / CH₂Cl₂ / 3 h / Ambient temperature

With pyridine; hydrogen; palladium on activated charcoal; In methanol; dichloromethane;

DOI:10.1016/S0968-0896(97)00096-5

Reference yield:

{4-[(1-Methyl-4-nitro-1H-pyrrole-2-carbonyl)-amino]-phenyl}-carbamic acid tert-butyl ester (197705-51-4) → [4-({1-Methyl-4-[(1-methyl-4-nitro-1H-pyrrole-2-carbonyl)-amino]-1H-pyrrole-2-carbonyl}-amino)-phenyl]-carbamic acid tert-butyl ester (197705-52-5)

Guidance literature:

Multi-step reaction with 2 steps

1: H₂ / 5percent Pd/C / methanol / 6 h / 760 Torr / Ambient temperature

2: pyridine / CH₂Cl₂ / 3 h / Ambient temperature

With pyridine; hydrogen; palladium on activated charcoal; In methanol; dichloromethane;

DOI:10.1016/S0968-0896(97)00096-5

upstream raw materials:

1-methyl-4-nitro-pyrrol-2-carboxylic acid

1-methyl-4-nitro-1H-pyrrole-2-carbonyl chloride

{4-[(1-Methyl-4-nitro-1H-pyrrole-2-carbonyl)-amino]-phenyl}-carbamic acid tert-butyl ester

Downstream raw materials:

(4-{[4-({4-[(4-{4-[Bis-(2-chloro-ethyl)-amino]-benzoylamino}-1-methyl-1H-pyrrole-2-carbonyl)-amino]-1-methyl-1H-pyrrole-2-carbonyl}-amino)-1-methyl-1H-pyrrole-2-carbonyl]-amino}-phenyl)-carbamic acid tert-butyl ester

(4-{[1-Methyl-4-({1-methyl-4-[(1-methyl-4-nitro-1H-pyrrole-2-carbonyl)-amino]-1H-pyrrole-2-carbonyl}-amino)-1H-pyrrole-2-carbonyl]-amino}-phenyl)-carbamic acid tert-butyl ester