(1R,2S,5R)-2-isopropyl-5-methylcyclohexyl 7-(2-amino-1H-imidazol-4-yl)heptylcarbamate hydrochloride

Base Information

Chemical Name:(1R,2S,5R)-2-isopropyl-5-methylcyclohexyl 7-(2-amino-1H-imidazol-4-yl)heptylcarbamate hydrochloride
CAS No.:1279724-09-2
Molecular Formula:C₂₁H₃₈N₄O₂*ClH
Molecular Weight:415.019
Hs Code.:

Synonyms:(1R,2S,5R)-2-isopropyl-5-methylcyclohexyl 7-(2-amino-1H-imidazol-4-yl)heptylcarbamate hydrochloride

Suppliers and Price of (1R,2S,5R)-2-isopropyl-5-methylcyclohexyl 7-(2-amino-1H-imidazol-4-yl)heptylcarbamate hydrochloride

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 (1R,2S,5R)-2-isopropyl-5-methylcyclohexyl 7-(2-amino-1H-imidazol-4-yl)heptylcarbamate hydrochloride

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of (1R,2S,5R)-2-isopropyl-5-methylcyclohexyl 7-(2-amino-1H-imidazol-4-yl)heptylcarbamate hydrochloride

There total 7 articles about (1R,2S,5R)-2-isopropyl-5-methylcyclohexyl 7-(2-amino-1H-imidazol-4-yl)heptylcarbamate hydrochloride 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:

: 1279724-31-0
(1R,2S,5R)-2-isopropyl-5-methylcyclohexyl 7-(2-amino-1H-imidazol-4-yl)heptylcarbamate

: 1279724-09-2
(1R,2S,5R)-2-isopropyl-5-methylcyclohexyl 7-(2-amino-1H-imidazol-4-yl)heptylcarbamate hydrochloride

Guidance literature:: With hydrogenchloride; In methanol;
DOI:10.1016/j.bmcl.2010.12.057

Reference yield:

: 217180-77-3
8-azidooctanoyl chloride

: 1279724-09-2
(1R,2S,5R)-2-isopropyl-5-methylcyclohexyl 7-(2-amino-1H-imidazol-4-yl)heptylcarbamate hydrochloride

Guidance literature:: Multi-step reaction with 6 steps

1: dichloromethane / 1 h / 0 °C

2: N,N-dimethyl-formamide / 48 h

3: palladium 10% on activated carbon; hydrogen / methanol

4: triethylamine / dichloromethane / 0 - 20 °C

5: trifluoroacetic acid / dichloromethane / 16 h

6: hydrogenchloride / methanol

With hydrogenchloride; palladium 10% on activated carbon; hydrogen; triethylamine; trifluoroacetic acid; In methanol; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1016/j.bmcl.2010.12.057

Reference yield:

: 1279724-16-1
9-azido-1-bromononan-2-one

: 1279724-09-2
(1R,2S,5R)-2-isopropyl-5-methylcyclohexyl 7-(2-amino-1H-imidazol-4-yl)heptylcarbamate hydrochloride

Guidance literature:: Multi-step reaction with 5 steps

1: N,N-dimethyl-formamide / 48 h

2: palladium 10% on activated carbon; hydrogen / methanol

3: triethylamine / dichloromethane / 0 - 20 °C

4: trifluoroacetic acid / dichloromethane / 16 h

5: hydrogenchloride / methanol

With hydrogenchloride; palladium 10% on activated carbon; hydrogen; triethylamine; trifluoroacetic acid; In methanol; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1016/j.bmcl.2010.12.057