(3R,4R,5S)-5-[[(1Z)-[[(tert-butoxy)carbonyl]amino]([[(tert-butoxy)carbonyl]imino])methyl]amino]-4-acetylamino-3-(pent-3-yloxy)cyclohexyl-1-ene-1-carboxylic acid

Base Information

Chemical Name:(3R,4R,5S)-5-[[(1Z)-[[(tert-butoxy)carbonyl]amino]([[(tert-butoxy)carbonyl]imino])methyl]amino]-4-acetylamino-3-(pent-3-yloxy)cyclohexyl-1-ene-1-carboxylic acid
CAS No.:1192537-55-5
Molecular Formula:C₂₅H₄₂N₄O₈
Molecular Weight:526.63
Hs Code.:

(3R,4R,5S)-5-[[(1Z)-[[(tert-butoxy)carbonyl]amino]([[(tert-butoxy)carbonyl]imino])methyl]amino]-4-acetylamino-3-(pent-3-yloxy)cyclohexyl-1-ene-1-carboxylic acid

Synonyms:

Suppliers and Price of (3R,4R,5S)-5-[[(1Z)-[[(tert-butoxy)carbonyl]amino]([[(tert-butoxy)carbonyl]imino])methyl]amino]-4-acetylamino-3-(pent-3-yloxy)cyclohexyl-1-ene-1-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 (3R,4R,5S)-5-[[(1Z)-[[(tert-butoxy)carbonyl]amino]([[(tert-butoxy)carbonyl]imino])methyl]amino]-4-acetylamino-3-(pent-3-yloxy)cyclohexyl-1-ene-1-carboxylic acid

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of (3R,4R,5S)-5-[[(1Z)-[[(tert-butoxy)carbonyl]amino]([[(tert-butoxy)carbonyl]imino])methyl]amino]-4-acetylamino-3-(pent-3-yloxy)cyclohexyl-1-ene-1-carboxylic acid

There total 8 articles about (3R,4R,5S)-5-[[(1Z)-[[(tert-butoxy)carbonyl]amino]([[(tert-butoxy)carbonyl]imino])methyl]amino]-4-acetylamino-3-(pent-3-yloxy)cyclohexyl-1-ene-1-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:

: 101769-63-5
(3R,4S,5R)-3,4,5-trihydroxycyclohex-1-ene-1-carboxylic acid ethyl ester

: 1192537-55-5,1612184-40-3
(3R,4R,5S)-5-[[(1Z)-[[(tert-butoxy)carbonyl]amino]([[(tert-butoxy)carbonyl]imino])methyl]amino]-4-acetylamino-3-(pent-3-yloxy)cyclohexyl-1-ene-1-carboxylic acid

Guidance literature:: Multi-step reaction with 8 steps

1.1: dmap; triethylamine / ethyl acetate / 1.5 h / 0 °C

2.1: sodium azide / acetone; water / 4 h / 0 °C

3.1: toluene / 5.5 h / 120 °C / Reflux

3.2: 16 h / 20 °C / Cooling with ice

4.1: sulfuric acid / ethanol / 16 h / 70 °C

4.2: 4.5 h / 20 °C

5.1: sodium azide / water; ethanol / 8 h / Reflux

6.1: 5% Pd-CaCO3; hydrogen / ethanol / 16 h / 20 °C

7.1: triethylamine / dichloromethane

8.1: potassium hydroxide / water; 1,4-dioxane

8.2: amberlite IR-120 resin / 0.08 h

With dmap; sodium azide; sulfuric acid; 5% Pd-CaCO3; hydrogen; triethylamine; potassium hydroxide; In 1,4-dioxane; ethanol; dichloromethane; water; ethyl acetate; acetone; toluene;
DOI:10.1021/jm401977j

Reference yield:

: 138-59-0
shikimic acid

: 1192537-55-5,1612184-40-3
(3R,4R,5S)-5-[[(1Z)-[[(tert-butoxy)carbonyl]amino]([[(tert-butoxy)carbonyl]imino])methyl]amino]-4-acetylamino-3-(pent-3-yloxy)cyclohexyl-1-ene-1-carboxylic acid

Guidance literature:: Multi-step reaction with 9 steps

1.1: thionyl chloride / 2.5 h / 85 °C

2.1: dmap; triethylamine / ethyl acetate / 1.5 h / 0 °C

3.1: sodium azide / acetone; water / 4 h / 0 °C

4.1: toluene / 5.5 h / 120 °C / Reflux

4.2: 16 h / 20 °C / Cooling with ice

5.1: sulfuric acid / ethanol / 16 h / 70 °C

5.2: 4.5 h / 20 °C

6.1: sodium azide / water; ethanol / 8 h / Reflux

7.1: 5% Pd-CaCO3; hydrogen / ethanol / 16 h / 20 °C

8.1: triethylamine / dichloromethane

9.1: potassium hydroxide / water; 1,4-dioxane

9.2: amberlite IR-120 resin / 0.08 h

With dmap; thionyl chloride; sodium azide; sulfuric acid; 5% Pd-CaCO3; hydrogen; triethylamine; potassium hydroxide; In 1,4-dioxane; ethanol; dichloromethane; water; ethyl acetate; acetone; toluene;
DOI:10.1021/jm401977j

Reference yield:

: 1132659-94-9
(3R,4S,5R)-3,4,5-tris-methanesulfonyloxy-cyclohex-1-enecarboxylic acid ethyl ester

: 1192537-55-5,1612184-40-3
(3R,4R,5S)-5-[[(1Z)-[[(tert-butoxy)carbonyl]amino]([[(tert-butoxy)carbonyl]imino])methyl]amino]-4-acetylamino-3-(pent-3-yloxy)cyclohexyl-1-ene-1-carboxylic acid

Guidance literature:: Multi-step reaction with 7 steps

1.1: sodium azide / acetone; water / 4 h / 0 °C

2.1: toluene / 5.5 h / 120 °C / Reflux

2.2: 16 h / 20 °C / Cooling with ice

3.1: sulfuric acid / ethanol / 16 h / 70 °C

3.2: 4.5 h / 20 °C

4.1: sodium azide / water; ethanol / 8 h / Reflux

5.1: 5% Pd-CaCO3; hydrogen / ethanol / 16 h / 20 °C

6.1: triethylamine / dichloromethane

7.1: potassium hydroxide / water; 1,4-dioxane

7.2: amberlite IR-120 resin / 0.08 h

With sodium azide; sulfuric acid; 5% Pd-CaCO3; hydrogen; triethylamine; potassium hydroxide; In 1,4-dioxane; ethanol; dichloromethane; water; acetone; toluene;
DOI:10.1021/jm401977j