1-{1-[1-({2-benzyl-2-[(3-hydroxy-2,2-dimethyl-1-oxopropyl)amino]-1-oxopropyl}amino)cyclopentanecarboxamido]cyclopentanecarboxamido}-N,N-dimethylcyclopentanecarboxamide

Base Information

Chemical Name:1-{1-[1-({2-benzyl-2-[(3-hydroxy-2,2-dimethyl-1-oxopropyl)amino]-1-oxopropyl}amino)cyclopentanecarboxamido]cyclopentanecarboxamido}-N,N-dimethylcyclopentanecarboxamide
CAS No.:266338-90-3
Molecular Formula:C₃₅H₅₃N₅O₆
Molecular Weight:639.836
Hs Code.:

1-{1-[1-({2-benzyl-2-[(3-hydroxy-2,2-dimethyl-1-oxopropyl)amino]-1-oxopropyl}amino)cyclopentanecarboxamido]cyclopentanecarboxamido}-N,N-dimethylcyclopentanecarboxamide

Synonyms:1-{1-[1-({2-benzyl-2-[(3-hydroxy-2,2-dimethyl-1-oxopropyl)amino]-1-oxopropyl}amino)cyclopentanecarboxamido]cyclopentanecarboxamido}-N,N-dimethylcyclopentanecarboxamide

Suppliers and Price of 1-{1-[1-({2-benzyl-2-[(3-hydroxy-2,2-dimethyl-1-oxopropyl)amino]-1-oxopropyl}amino)cyclopentanecarboxamido]cyclopentanecarboxamido}-N,N-dimethylcyclopentanecarboxamide

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-{1-[1-({2-benzyl-2-[(3-hydroxy-2,2-dimethyl-1-oxopropyl)amino]-1-oxopropyl}amino)cyclopentanecarboxamido]cyclopentanecarboxamido}-N,N-dimethylcyclopentanecarboxamide

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 1-{1-[1-({2-benzyl-2-[(3-hydroxy-2,2-dimethyl-1-oxopropyl)amino]-1-oxopropyl}amino)cyclopentanecarboxamido]cyclopentanecarboxamido}-N,N-dimethylcyclopentanecarboxamide

There total 8 articles about 1-{1-[1-({2-benzyl-2-[(3-hydroxy-2,2-dimethyl-1-oxopropyl)amino]-1-oxopropyl}amino)cyclopentanecarboxamido]cyclopentanecarboxamido}-N,N-dimethylcyclopentanecarboxamide 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: 97.0%

: 108805-12-5
3'-(Dimethylamino)spiroazirin>

: 266338-86-7
1-[1-({2-benzyl-2-[(3-hydroxy-2,2-dimethyl-1-oxopropyl)amino]-1-oxopropyl}amino)cyclopentanecarboxamido]cyclopentanecarboxilic acid

: 266338-90-3
1-{1-[1-({2-benzyl-2-[(3-hydroxy-2,2-dimethyl-1-oxopropyl)amino]-1-oxopropyl}amino)cyclopentanecarboxamido]cyclopentanecarboxamido}-N,N-dimethylcyclopentanecarboxamide

Guidance literature:: In acetonitrile; at 20 ℃; for 26h;
DOI:10.1002/(SICI)1522-2675(20000119)83:1<233::AID-HLCA233>3.0.CO;2-1

Reference yield:

: 4835-90-9
3-Hydroxy-2,2-dimethylpropanoic acid

: 266338-90-3
1-{1-[1-({2-benzyl-2-[(3-hydroxy-2,2-dimethyl-1-oxopropyl)amino]-1-oxopropyl}amino)cyclopentanecarboxamido]cyclopentanecarboxamido}-N,N-dimethylcyclopentanecarboxamide

Guidance literature:: Multi-step reaction with 7 steps

1: 97 percent / acetonitrile / 30 h / 20 °C

2: 95 percent / aq. HCl / tetrahydrofuran / 26 h / 20 °C

3: 92 percent / acetonitrile / 25 h / 20 °C

4: 86 percent / aq. HCl / tetrahydrofuran / 5 h / 20 °C

5: 99 percent / acetonitrile / 72 h / 20 °C

6: 98 percent / aq. HCl / tetrahydrofuran / 23 h / 20 °C

7: 97 percent / acetonitrile / 26 h / 20 °C

With hydrogenchloride; In tetrahydrofuran; acetonitrile; 1: Addition / 2: Hydrolysis / 3: Addition / 4: Hydrolysis / 5: Addition / 6: Hydrolysis / 7: Addition;
DOI:10.1002/(SICI)1522-2675(20000119)83:1<233::AID-HLCA233>3.0.CO;2-1

Reference yield:

: 114234-21-8
2-benzyl-3-(dimethylamino)-2-methyl-2H-azirine

: 266338-90-3
1-{1-[1-({2-benzyl-2-[(3-hydroxy-2,2-dimethyl-1-oxopropyl)amino]-1-oxopropyl}amino)cyclopentanecarboxamido]cyclopentanecarboxamido}-N,N-dimethylcyclopentanecarboxamide

Guidance literature:: Multi-step reaction with 7 steps

1: 97 percent / acetonitrile / 30 h / 20 °C

2: 95 percent / aq. HCl / tetrahydrofuran / 26 h / 20 °C

3: 92 percent / acetonitrile / 25 h / 20 °C

4: 86 percent / aq. HCl / tetrahydrofuran / 5 h / 20 °C

5: 99 percent / acetonitrile / 72 h / 20 °C

6: 98 percent / aq. HCl / tetrahydrofuran / 23 h / 20 °C

7: 97 percent / acetonitrile / 26 h / 20 °C

With hydrogenchloride; In tetrahydrofuran; acetonitrile; 1: Addition / 2: Hydrolysis / 3: Addition / 4: Hydrolysis / 5: Addition / 6: Hydrolysis / 7: Addition;
DOI:10.1002/(SICI)1522-2675(20000119)83:1<233::AID-HLCA233>3.0.CO;2-1