ethyl 4-({4-[({6-[cyclohexyl(cyclopropylmethyl)amino]pyrimidin-4-yl}carbonyl)amino]phenyl}sulfonyl)butanoate

Base Information

Chemical Name:ethyl 4-({4-[({6-[cyclohexyl(cyclopropylmethyl)amino]pyrimidin-4-yl}carbonyl)amino]phenyl}sulfonyl)butanoate
CAS No.:1114591-69-3
Molecular Formula:C₂₇H₃₆N₄O₅S
Molecular Weight:528.673
Hs Code.:

Synonyms:ethyl 4-({4-[({6-[cyclohexyl(cyclopropylmethyl)amino]pyrimidin-4-yl}carbonyl)amino]phenyl}sulfonyl)butanoate

Suppliers and Price of ethyl 4-({4-[({6-[cyclohexyl(cyclopropylmethyl)amino]pyrimidin-4-yl}carbonyl)amino]phenyl}sulfonyl)butanoate

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 ethyl 4-({4-[({6-[cyclohexyl(cyclopropylmethyl)amino]pyrimidin-4-yl}carbonyl)amino]phenyl}sulfonyl)butanoate

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of ethyl 4-({4-[({6-[cyclohexyl(cyclopropylmethyl)amino]pyrimidin-4-yl}carbonyl)amino]phenyl}sulfonyl)butanoate

There total 9 articles about ethyl 4-({4-[({6-[cyclohexyl(cyclopropylmethyl)amino]pyrimidin-4-yl}carbonyl)amino]phenyl}sulfonyl)butanoate 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:

: 1114592-38-9
ethyl 4-(4-aminophenylsulfonyl)butanoate

: 1114592-08-3
6-[cyclohexyl(cyclopropylmethyl)amino]pyrimidine-4-carboxylic acid

: 1114591-69-3
ethyl 4-({4-[({6-[cyclohexyl(cyclopropylmethyl)amino]pyrimidin-4-yl}carbonyl)amino]phenyl}sulfonyl)butanoate

Guidance literature:: 6-[cyclohexyl(cyclopropylmethyl)amino]pyrimidine-4-carboxylic acid; With diisopropylamine; methyl chloroformate; In dichloromethane; at 0 ℃; for 0.25h;

ethyl 4-(4-aminophenylsulfonyl)butanoate; In dichloromethane; at 0 - 20 ℃; for 1.5h;

Reference yield:

: 2969-81-5
Ethyl 4-bromobutyrate

: 1114591-69-3
ethyl 4-({4-[({6-[cyclohexyl(cyclopropylmethyl)amino]pyrimidin-4-yl}carbonyl)amino]phenyl}sulfonyl)butanoate

Guidance literature:: Multi-step reaction with 4 steps

1.1: potassium carbonate / acetone / 18 h / 20 °C

2.1: 3-chloro-benzenecarboperoxoic acid / 72 h / 20 °C

3.1: hydrogen / 5%-palladium/activated carbon / ethanol / 18 h

4.1: diisopropylamine; methyl chloroformate / dichloromethane / 0.25 h / 0 °C

4.2: 1.5 h / 0 - 20 °C

With hydrogen; potassium carbonate; diisopropylamine; methyl chloroformate; 3-chloro-benzenecarboperoxoic acid; 5%-palladium/activated carbon; In ethanol; dichloromethane; acetone;

Reference yield:

: 1114592-06-1
methyl 2-chloro-6-[cyclohexyl(cyclopropylmethyl)amino]pyrimidine-4-carboxylate

: 1114591-69-3
ethyl 4-({4-[({6-[cyclohexyl(cyclopropylmethyl)amino]pyrimidin-4-yl}carbonyl)amino]phenyl}sulfonyl)butanoate

Guidance literature:: Multi-step reaction with 3 steps

1.1: ammonium formate / palladium 10% on activated carbon / water; isopropyl alcohol / 0.75 h / 20 °C

2.1: lithium hydroxide; water / tetrahydrofuran; ethanol / 1 h / 20 °C

2.2: pH 6

3.1: diisopropylamine; methyl chloroformate / dichloromethane / 0.25 h / 0 °C

3.2: 1.5 h / 0 - 20 °C

With lithium hydroxide; water; ammonium formate; diisopropylamine; methyl chloroformate; palladium 10% on activated carbon; In tetrahydrofuran; ethanol; dichloromethane; water; isopropyl alcohol;