tert-butyl {2-(benzyloxy)-2-[3-(4-chlorophenyl)-1-(pyrimidin-2-yl)-1H-pyrazol-5-yl]ethyl}carbamate

Base Information

Chemical Name:tert-butyl {2-(benzyloxy)-2-[3-(4-chlorophenyl)-1-(pyrimidin-2-yl)-1H-pyrazol-5-yl]ethyl}carbamate
CAS No.:1350881-23-0
Molecular Formula:C₂₇H₂₈ClN₅O₃
Molecular Weight:506.004
Hs Code.:

Synonyms:tert-butyl {2-(benzyloxy)-2-[3-(4-chlorophenyl)-1-(pyrimidin-2-yl)-1H-pyrazol-5-yl]ethyl}carbamate

Suppliers and Price of tert-butyl {2-(benzyloxy)-2-[3-(4-chlorophenyl)-1-(pyrimidin-2-yl)-1H-pyrazol-5-yl]ethyl}carbamate

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 tert-butyl {2-(benzyloxy)-2-[3-(4-chlorophenyl)-1-(pyrimidin-2-yl)-1H-pyrazol-5-yl]ethyl}carbamate

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of tert-butyl {2-(benzyloxy)-2-[3-(4-chlorophenyl)-1-(pyrimidin-2-yl)-1H-pyrazol-5-yl]ethyl}carbamate

There total 7 articles about tert-butyl {2-(benzyloxy)-2-[3-(4-chlorophenyl)-1-(pyrimidin-2-yl)-1H-pyrazol-5-yl]ethyl}carbamate 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:

: 1350881-22-9
tert-butyl {2-(benzyloxy)-2-[3-(4-chloropheny)-1H-pyrazol-5-yl]ethyl}carbamate

: 4595-60-2
2-bromopyrimidine

: 1350881-23-0
tert-butyl {2-(benzyloxy)-2-[3-(4-chlorophenyl)-1-(pyrimidin-2-yl)-1H-pyrazol-5-yl]ethyl}carbamate

Guidance literature:: With 1,10-Phenanthroline; caesium carbonate; copper(l) iodide; at 120 ℃; for 2h; Inert atmosphere;

Reference yield:

: 24424-99-5
di-tert-butyl dicarbonate

: 1350881-23-0
tert-butyl {2-(benzyloxy)-2-[3-(4-chlorophenyl)-1-(pyrimidin-2-yl)-1H-pyrazol-5-yl]ethyl}carbamate

Guidance literature:: Multi-step reaction with 7 steps

1.1: sodium hydroxide / 1,4-dioxane / 0 - 20 °C

2.1: sodium hydride / N,N-dimethyl-formamide; mineral oil / 1 h / 0 °C

2.2: 0 - 20 °C

3.1: sodium hydroxide; water / 1,4-dioxane / 50 °C

4.1: triethylamine; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol / dichloromethane / 20 °C

5.1: n-butyllithium / hexane; tetrahydrofuran / 1 h / -78 °C

5.2: 1.5 h / -78 - 0 °C

6.1: hydrazine / ethanol / 3 h / 75 °C

7.1: caesium carbonate; 1,10-Phenanthroline / copper(l) iodide / 2 h / 120 °C / Inert atmosphere

With n-butyllithium; 1,10-Phenanthroline; water; sodium hydride; benzotriazol-1-ol; caesium carbonate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; sodium hydroxide; hydrazine; copper(l) iodide; In tetrahydrofuran; 1,4-dioxane; ethanol; hexane; dichloromethane; N,N-dimethyl-formamide; mineral oil;

Reference yield:

: 1350881-19-4
benzyl 2-(benzyloxy)-3-[(tert-butoxycarbonyl)amino]propanoate

: 1350881-23-0
tert-butyl {2-(benzyloxy)-2-[3-(4-chlorophenyl)-1-(pyrimidin-2-yl)-1H-pyrazol-5-yl]ethyl}carbamate

Guidance literature:: Multi-step reaction with 5 steps

1.1: sodium hydroxide; water / 1,4-dioxane / 50 °C

2.1: triethylamine; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol / dichloromethane / 20 °C

3.1: n-butyllithium / hexane; tetrahydrofuran / 1 h / -78 °C

3.2: 1.5 h / -78 - 0 °C

4.1: hydrazine / ethanol / 3 h / 75 °C

5.1: caesium carbonate; 1,10-Phenanthroline / copper(l) iodide / 2 h / 120 °C / Inert atmosphere

With n-butyllithium; 1,10-Phenanthroline; water; benzotriazol-1-ol; caesium carbonate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; sodium hydroxide; hydrazine; copper(l) iodide; In tetrahydrofuran; 1,4-dioxane; ethanol; hexane; dichloromethane;