ethyl 2-(diphenylmethyleneamino)-7-(1-(2-(4-pentylbenzamido)ethyl)-1H-1,2,3-triazol-4-yl)heptanoate

Base Information

Chemical Name:ethyl 2-(diphenylmethyleneamino)-7-(1-(2-(4-pentylbenzamido)ethyl)-1H-1,2,3-triazol-4-yl)heptanoate
CAS No.:1421703-95-8
Molecular Formula:C₃₈H₄₇N₅O₃
Molecular Weight:621.823
Hs Code.:

Synonyms:ethyl 2-(diphenylmethyleneamino)-7-(1-(2-(4-pentylbenzamido)ethyl)-1H-1,2,3-triazol-4-yl)heptanoate

Suppliers and Price of ethyl 2-(diphenylmethyleneamino)-7-(1-(2-(4-pentylbenzamido)ethyl)-1H-1,2,3-triazol-4-yl)heptanoate

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 2-(diphenylmethyleneamino)-7-(1-(2-(4-pentylbenzamido)ethyl)-1H-1,2,3-triazol-4-yl)heptanoate

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of ethyl 2-(diphenylmethyleneamino)-7-(1-(2-(4-pentylbenzamido)ethyl)-1H-1,2,3-triazol-4-yl)heptanoate

There total 2 articles about ethyl 2-(diphenylmethyleneamino)-7-(1-(2-(4-pentylbenzamido)ethyl)-1H-1,2,3-triazol-4-yl)heptanoate 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: 84.0%

: 1192358-22-7
N-(2-azidoethyl)-4-pentylbenzamide

: 1353046-53-3
ethyl 2-(diphenylmethyleneamino)non-8-ynoate

: 1421703-95-8
ethyl 2-(diphenylmethyleneamino)-7-(1-(2-(4-pentylbenzamido)ethyl)-1H-1,2,3-triazol-4-yl)heptanoate

Guidance literature:: With copper(II) sulfate; sodium L-ascorbate; In dichloromethane; water; tert-butyl alcohol; at 20 ℃; for 12h;
DOI:10.1002/cmdc.201200350

Reference yield:

: 69555-14-2
ethyl N-diphenylmethylene glycine

: 87462-66-6
1-iodo-6-heptyne

: 1421703-95-8
ethyl 2-(diphenylmethyleneamino)-7-(1-(2-(4-pentylbenzamido)ethyl)-1H-1,2,3-triazol-4-yl)heptanoate

Guidance literature:: Multi-step reaction with 2 steps

1: potassium tert-butylate / tetrahydrofuran / 2 h / -78 - 20 °C

2: copper(II) sulfate; sodium L-ascorbate / water; ethanol; dichloromethane / 3 h / 20 °C

With potassium tert-butylate; copper(II) sulfate; sodium L-ascorbate; In tetrahydrofuran; ethanol; dichloromethane; water; 2: |Huisgen Cycloaddition;
DOI:10.1002/anie.201206911

Reference yield: 95.0%

: 1421703-95-8
ethyl 2-(diphenylmethyleneamino)-7-(1-(2-(4-pentylbenzamido)ethyl)-1H-1,2,3-triazol-4-yl)heptanoate

: 6638-79-5
N,O-dimethylhydroxylamine*hydrochloride

: 1421703-96-9
N-(2-(4-(6-(diphenylmethyleneamino)-7-(methoxy-(methyl)amino)-7-oxoheptyl)-1H-1,2,3-triazol-1-yl)ethyl)-4-pentylbenzamide

Guidance literature:: With isopropylmagnesium chloride; In tetrahydrofuran; at -20 - 0 ℃; for 3h; Inert atmosphere;
DOI:10.1002/cmdc.201200350