1-(cyclohexylmethyl)-2-methyl-5-(1-(piperidin-1-ylsulfonyl)indolizin-3-yl)-1H-pyrrole-3-carboxylic acid

Base Information

Chemical Name:1-(cyclohexylmethyl)-2-methyl-5-(1-(piperidin-1-ylsulfonyl)indolizin-3-yl)-1H-pyrrole-3-carboxylic acid
CAS No.:1442432-62-3
Molecular Formula:C₂₆H₃₃N₃O₄S
Molecular Weight:483.632
Hs Code.:

Synonyms:1-(cyclohexylmethyl)-2-methyl-5-(1-(piperidin-1-ylsulfonyl)indolizin-3-yl)-1H-pyrrole-3-carboxylic acid

Suppliers and Price of 1-(cyclohexylmethyl)-2-methyl-5-(1-(piperidin-1-ylsulfonyl)indolizin-3-yl)-1H-pyrrole-3-carboxylic acid

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of 1-(cyclohexylmethyl)-2-methyl-5-(1-(piperidin-1-ylsulfonyl)indolizin-3-yl)-1H-pyrrole-3-carboxylic acid

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 1-(cyclohexylmethyl)-2-methyl-5-(1-(piperidin-1-ylsulfonyl)indolizin-3-yl)-1H-pyrrole-3-carboxylic acid

There total 7 articles about 1-(cyclohexylmethyl)-2-methyl-5-(1-(piperidin-1-ylsulfonyl)indolizin-3-yl)-1H-pyrrole-3-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: 80.0%

: 1442432-61-2
ethyl 1-(cyclohexylmethyl)-2-methyl-5-(1-(piperidin-1-ylsulfonyl)indolizin-3-yl)-1H-pyrrole-3-carboxylate

: 1442432-62-3
1-(cyclohexylmethyl)-2-methyl-5-(1-(piperidin-1-ylsulfonyl)indolizin-3-yl)-1H-pyrrole-3-carboxylic acid

Guidance literature:: With potassium tert-butylate; water; In dimethyl sulfoxide; at 85 ℃; for 4h;

Reference yield:

: 1442432-59-8
ethyl 1-(cyclohexylmethyl)-2-methyl-5-(3-(pyridin-2-yl)propanoyl)-1H-pyrrole-3-carboxylate

: 1442432-62-3
1-(cyclohexylmethyl)-2-methyl-5-(1-(piperidin-1-ylsulfonyl)indolizin-3-yl)-1H-pyrrole-3-carboxylic acid

Guidance literature:: Multi-step reaction with 3 steps

1: toluene / 0.5 h / Dean-Stark; Inert atmosphere; Reflux

2: potassium carbonate / acetonitrile / Reflux

3: potassium tert-butylate; water / dimethyl sulfoxide / 4 h / 85 °C

With potassium tert-butylate; water; potassium carbonate; In dimethyl sulfoxide; toluene; acetonitrile;

Reference yield:

: 1442432-57-6
ethyl 5-acetyl-1-(cyclohexylmethyl)-2-methyl-1H-pyrrole-3-carboxylate

: 1442432-62-3
1-(cyclohexylmethyl)-2-methyl-5-(1-(piperidin-1-ylsulfonyl)indolizin-3-yl)-1H-pyrrole-3-carboxylic acid

Guidance literature:: Multi-step reaction with 5 steps

1: 1,8-diazabicyclo[5.4.0]undec-7-ene / tetrahydrofuran / 72 h / 20 °C

2: palladium on activated charcoal; hydrogen / methanol / 20 °C / 775.74 Torr

3: toluene / 0.5 h / Dean-Stark; Inert atmosphere; Reflux

4: potassium carbonate / acetonitrile / Reflux

5: potassium tert-butylate; water / dimethyl sulfoxide / 4 h / 85 °C

With palladium on activated charcoal; potassium tert-butylate; water; hydrogen; potassium carbonate; 1,8-diazabicyclo[5.4.0]undec-7-ene; In tetrahydrofuran; methanol; dimethyl sulfoxide; toluene; acetonitrile;