Ethyl 4-[(benzyloxycarbonyl)amino]-3-methoxy-1-methyl-1H-pyrrole-2-carboxylate

Base Information

• Chemical Name: Ethyl 4-[(benzyloxycarbonyl)amino]-3-methoxy-1-methyl-1H-pyrrole-2-carboxylate
• CAS No.: 285137-95-3
• Molecular Formula: C₁₇H₂₀N₂O₅
• Molecular Weight: 332.356
• Mol file: 285137-95-3.mol

Synonyms:Ethyl 4-[(benzyloxycarbonyl)amino]-3-methoxy-1-methyl-1H-pyrrole-2-carboxylate

Chemical Property of Ethyl 4-[(benzyloxycarbonyl)amino]-3-methoxy-1-methyl-1H-pyrrole-2-carboxylate

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
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MSDS Files:

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Technology Process of Ethyl 4-[(benzyloxycarbonyl)amino]-3-methoxy-1-methyl-1H-pyrrole-2-carboxylate

There total 8 articles about Ethyl 4-[(benzyloxycarbonyl)amino]-3-methoxy-1-methyl-1H-pyrrole-2-carboxylate 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-[(benzyloxycarbonyl)amino]-3-hydroxy-1-methylpyrrole-2-carboxylate (212184-25-3) + methyl iodide (74-88-4) → Ethyl 4-[(benzyloxycarbonyl)amino]-3-methoxy-1-methyl-1H-pyrrole-2-carboxylate (285137-95-3)

Guidance literature:

With dmap; potassium carbonate; In acetone; at 22 ℃; for 22h;

DOI:10.1021/ja9930667

Reference yield:

ethyl 4-carboxy-3-hydroxy-1-methylpyrrole-2-carboxylate (65171-82-6) → Ethyl 4-[(benzyloxycarbonyl)amino]-3-methoxy-1-methyl-1H-pyrrole-2-carboxylate (285137-95-3)

Guidance literature:

Multi-step reaction with 2 steps

1.1: Et₃N; DPPA / acetonitrile / 5 h / Heating

1.2: 53 percent / acetonitrile / 17 h / Heating

2.1: K₂CO₃; DMAP / acetone / 22 h / 22 °C

With dmap; diphenyl-phosphinic acid; potassium carbonate; triethylamine; In acetone; acetonitrile; 1.1: Curtius rearrangement / 1.2: Addition / 2.1: Methylation;

DOI:10.1021/ja9930667

Reference yield:

benzyl alcohol (100-51-6,185532-71-2) → Ethyl 4-[(benzyloxycarbonyl)amino]-3-methoxy-1-methyl-1H-pyrrole-2-carboxylate (285137-95-3)

Guidance literature:

Multi-step reaction with 2 steps

1.1: Et₃N; DPPA / acetonitrile / 5 h / Heating

1.2: 53 percent / acetonitrile / 17 h / Heating

2.1: K₂CO₃; DMAP / acetone / 22 h / 22 °C

With dmap; diphenyl-phosphinic acid; potassium carbonate; triethylamine; In acetone; acetonitrile; 1.1: Curtius rearrangement / 1.2: Addition / 2.1: Methylation;

DOI:10.1021/ja9930667

upstream raw materials:

benzyl alcohol

ethyl 4-[(benzyloxycarbonyl)amino]-3-hydroxy-1-methylpyrrole-2-carboxylate

methyl iodide

3-hydroxy-1-methyl-pyrrole-2,4-dicarboxylic acid diethyl ester

Downstream raw materials:

4-[(tert-butoxycarbonyl)amino]-3-methoxy-1-methylpyrrole-2-carboxylic acid