3-(5-((1R,2R)-2-aminocyclohexylamino)-5-oxopentyl)-1-methyl-1H-imidazol-3-iumhexafluorophosphate

Base Information

Chemical Name:3-(5-((1R,2R)-2-aminocyclohexylamino)-5-oxopentyl)-1-methyl-1H-imidazol-3-iumhexafluorophosphate
CAS No.:1438415-80-5
Molecular Formula:C₁₅H₂₇N₄O*F₆P
Molecular Weight:424.37
Hs Code.:

Synonyms:3-(5-((1R,2R)-2-aminocyclohexylamino)-5-oxopentyl)-1-methyl-1H-imidazol-3-iumhexafluorophosphate

Suppliers and Price of 3-(5-((1R,2R)-2-aminocyclohexylamino)-5-oxopentyl)-1-methyl-1H-imidazol-3-iumhexafluorophosphate

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 3-(5-((1R,2R)-2-aminocyclohexylamino)-5-oxopentyl)-1-methyl-1H-imidazol-3-iumhexafluorophosphate

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 3-(5-((1R,2R)-2-aminocyclohexylamino)-5-oxopentyl)-1-methyl-1H-imidazol-3-iumhexafluorophosphate

There total 4 articles about 3-(5-((1R,2R)-2-aminocyclohexylamino)-5-oxopentyl)-1-methyl-1H-imidazol-3-iumhexafluorophosphate 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: 98.0%

: 1438415-84-9
1-(5-((1R,2R)-2-(benzyloxycarbonylamino)cyclohexylamino)-5-oxopentyl)-3-methyl-1H-imidazol-3-ium hexafluorophosphate

: 1438415-80-5
3-(5-((1R,2R)-2-aminocyclohexylamino)-5-oxopentyl)-1-methyl-1H-imidazol-3-iumhexafluorophosphate

Guidance literature:: With 5%-palladium/activated carbon; hydrogen; In methanol; at 20 ℃; for 2h;
DOI:10.1002/adsc.201200338

Reference yield:

: 1438415-81-6
benzyl (1R,2R)-2-(5-bromopentanamido)cyclohexylcarbamate

: 1438415-80-5
3-(5-((1R,2R)-2-aminocyclohexylamino)-5-oxopentyl)-1-methyl-1H-imidazol-3-iumhexafluorophosphate

Guidance literature:: Multi-step reaction with 3 steps

1: 0.17 h / 80 °C

2: potassium hexafluorophosphate / water

3: hydrogen; 5%-palladium/activated carbon / methanol / 2 h / 20 °C

With potassium hexafluorophosphate; 5%-palladium/activated carbon; hydrogen; In methanol; water;
DOI:10.1002/adsc.201200338

Reference yield:

: 142350-85-4,1353973-30-4,445479-92-5
benzyl N-[(1R,2R)-2-aminocyclohexyl]carbamate

: 1438415-80-5
3-(5-((1R,2R)-2-aminocyclohexylamino)-5-oxopentyl)-1-methyl-1H-imidazol-3-iumhexafluorophosphate

Guidance literature:: Multi-step reaction with 4 steps

1: triethylamine / tetrahydrofuran / 2 h / 5 - 20 °C

2: 0.17 h / 80 °C

3: potassium hexafluorophosphate / water

4: hydrogen; 5%-palladium/activated carbon / methanol / 2 h / 20 °C

With potassium hexafluorophosphate; 5%-palladium/activated carbon; hydrogen; triethylamine; In tetrahydrofuran; methanol; water;
DOI:10.1002/adsc.201200338