9H-Pyrrolo[1,2-a]indole-2-carboxylic acid, 3-methyl-9-oxo-, ethyl ester

Base Information

• Chemical Name: 9H-Pyrrolo[1,2-a]indole-2-carboxylic acid, 3-methyl-9-oxo-, ethyl ester
• CAS No.: 60706-06-1
• Molecular Formula: C₁₅H₁₃NO₃
• Molecular Weight: 255.273
• DSSTox Substance ID: DTXSID70390506
• Wikidata: Q82187317
• ChEMBL ID: CHEMBL1486458
• Mol file: 60706-06-1.mol

Synonyms:60706-06-1;SMR000019966;ChemDiv2_001679;9H-Pyrrolo[1,2-a]indole-2-carboxylic acid, 3-methyl-9-oxo-, ethyl ester;MLS000043347;CHEMBL1486458;DTXSID70390506;HMS1373M07;HMS2400G18;SR-01000085155;SR-01000085155-1;ethyl 3-methyl-9-oxo-9H-pyrrolo[1,2-a]indole-2-carboxylate

Chemical Property of 9H-Pyrrolo[1,2-a]indole-2-carboxylic acid, 3-methyl-9-oxo-, ethyl ester

Chemical Property:

• XLogP3: 2.8
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 3
• Exact Mass: 255.08954328
• Heavy Atom Count: 19
• Complexity: 395

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCOC(=O)C1=C(N2C3=CC=CC=C3C(=O)C2=C1)C

Technology Process of 9H-Pyrrolo[1,2-a]indole-2-carboxylic acid, 3-methyl-9-oxo-, ethyl ester

There total 1 articles about 9H-Pyrrolo[1,2-a]indole-2-carboxylic acid, 3-methyl-9-oxo-, ethyl 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: 7.0%

1H-3-ethoxycarbonyl-2-methyl-1-(p-nitrophenyl)pyrido[3,2-b]indole (374697-64-0) → 2-ethoxycarbonyl-1-methyl-4-oxo-4H-pyrrolo[1,2-a]indole (60706-06-1) + 2-ethoxycarbonyl-1-methyl-4-p-nitrophenylimino-4H-pyrrolo[1,2-a]indole

Guidance literature:

With piperidine; In ethanol; at 100 ℃; for 9h;

DOI:10.1023/A:1025110602750

upstream raw materials:

1H-3-ethoxycarbonyl-2-methyl-1-(p-nitrophenyl)pyrido[3,2-b]indole