4-<(tert-butyloxycarbonyl)amino>-1,3,5-trimethylpyrrole-2-carboxylic acid

Base Information

• Chemical Name: 4-<(tert-butyloxycarbonyl)amino>-1,3,5-trimethylpyrrole-2-carboxylic acid
• CAS No.: 75792-48-2
• Molecular Formula: C₁₃H₂₀N₂O₄
• Molecular Weight: 268.313
• Mol file: 75792-48-2.mol

Synonyms:4-<(tert-butyloxycarbonyl)amino>-1,3,5-trimethylpyrrole-2-carboxylic acid

Chemical Property of 4-<(tert-butyloxycarbonyl)amino>-1,3,5-trimethylpyrrole-2-carboxylic acid

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 4-<(tert-butyloxycarbonyl)amino>-1,3,5-trimethylpyrrole-2-carboxylic acid

There total 8 articles about 4-<(tert-butyloxycarbonyl)amino>-1,3,5-trimethylpyrrole-2-carboxylic acid 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:

ethyl 4-carboxy-1,3,5-trimethylpyrrole-2-carboxylate (7473-16-7) → 4-<(tert-butyloxycarbonyl)amino>-1,3,5-trimethylpyrrole-2-carboxylic acid (75792-48-2)

Guidance literature:

Multi-step reaction with 4 steps

1: 100 percent / NaH / 90 °C / 10 Torr

2: 75 percent / diphenylphosphoryl azide (DPPA), Et₃N / acetonitrile / 1.5 h / 50 °C

3: 95 percent / CuCl / 5 h / 60 °C

4: H₂ / 10percent Pd/C / dioxane / 12 h

With diphenylphosphoranyl azide; hydrogen; sodium hydride; triethylamine; copper(l) chloride; palladium on activated charcoal; In 1,4-dioxane; acetonitrile;

DOI:10.1021/jm00133a008

Reference yield:

benzyl 4-<(tert-butyloxycarbonyl)amino>-1,3,5-trimethylpyrrole-2-carboxylate (75792-47-1) → 4-<(tert-butyloxycarbonyl)amino>-1,3,5-trimethylpyrrole-2-carboxylic acid (75792-48-2)

Guidance literature:

With hydrogen; palladium on activated charcoal; In 1,4-dioxane; for 12h;

DOI:10.1021/jm00133a008

Reference yield:

N-(tert-butyloxycarbonyl) azide (1070-19-5) → 4-<(tert-butyloxycarbonyl)amino>-1,3,5-trimethylpyrrole-2-carboxylic acid (75792-48-2)

Guidance literature:

Multi-step reaction with 2 steps

2: H₂ / 10percent Pd/C / dioxane / 12 h

With hydrogen; palladium on activated charcoal; In 1,4-dioxane;

DOI:10.1021/jm00133a008

upstream raw materials:

benzyl 4-<(tert-butyloxycarbonyl)amino>-1,3,5-trimethylpyrrole-2-carboxylate

N-(tert-butyloxycarbonyl) azide

ethyl 4-carboxy-1,3,5-trimethylpyrrole-2-carboxylate

ethyl 4-isocyanato-1,3,5-trimethylpyrrole-2-carboxylate

Downstream raw materials:

N-<5-<<(3-amino-3-iminopropyl)amino>carbonyl>-1,2,4-trimethylpyrrol-3-yl>-4-<<<4-(formylamino)-1,3,5-trimethylpyrrol-2-yl>carbonyl>amino>-1,3,5-trimethylpyrrole-2-carboxamide hydrochloride

N-<5-(benzyloxycarbonyl)-1,2,4-trimethylpyrrol-3-yl>-4-<<<4-<(tert-butyloxycarbonyl)amino>-1,3,5-trimethylpyrrol-2-yl>carbonyl>amino>-1,3,5-trimethylpyrrole-2-carboxamide

N-<5-(benzyloxycarbonyl)-1,2,4-trimethylpyrrol-3-yl>-4-<(tert-butyloxycarbonyl)amino>-1,3,5-trimethylpyrrole-2-carboxamide