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

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Chemical Name:tert-butyl {2-[3-(4-chlorophenyl)-1H-(pyrimidin-2-yl)-1H-pyrazol-5-yl]-2-hydroxyethyl}(1-hydroxy-4-phenylbutan-2-yl)carbamate
CAS No.:1350881-14-9
Molecular Formula:C₃₀H₃₄ClN₅O₄
Molecular Weight:564.084
Hs Code.:

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

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Chemical Property of tert-butyl {2-[3-(4-chlorophenyl)-1H-(pyrimidin-2-yl)-1H-pyrazol-5-yl]-2-hydroxyethyl}(1-hydroxy-4-phenylbutan-2-yl)carbamate

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

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

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

: 1350881-25-2
2-({2-[3-(4-chlorophenyl)-1-(pyrimidin-2-yl)-1H-pyrazoI-5-yl]-2-hydroxyethyl}amino)-4-phenylbutan-1-ol

: 1350881-14-9
tert-butyl {2-[3-(4-chlorophenyl)-1H-(pyrimidin-2-yl)-1H-pyrazol-5-yl]-2-hydroxyethyl}(1-hydroxy-4-phenylbutan-2-yl)carbamate

Guidance literature:: With triethylamine; In methanol; at 50 ℃; for 2h;

Reference yield:

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

: 1350881-14-9
tert-butyl {2-[3-(4-chlorophenyl)-1H-(pyrimidin-2-yl)-1H-pyrazol-5-yl]-2-hydroxyethyl}(1-hydroxy-4-phenylbutan-2-yl)carbamate

Guidance literature:: Multi-step reaction with 4 steps

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

2.1: boron tribromide / dichloromethane / 0.67 h / 0 °C

2.2: 0.5 h

3.1: sodium tris(acetoxy)borohydride / 1,2-dichloro-ethane / 6 h / 20 °C

4.1: triethylamine / methanol / 2 h / 50 °C

With 1,10-Phenanthroline; boron tribromide; sodium tris(acetoxy)borohydride; caesium carbonate; triethylamine; copper(l) iodide; In methanol; dichloromethane; 1,2-dichloro-ethane;

Reference yield:

: 1350881-21-8
tert-butyl [2-(benzyloxy)-5-(4-chlorophenyI)-3-oxopent-4-yn-1-yl]carbamate

: 1350881-14-9
tert-butyl {2-[3-(4-chlorophenyl)-1H-(pyrimidin-2-yl)-1H-pyrazol-5-yl]-2-hydroxyethyl}(1-hydroxy-4-phenylbutan-2-yl)carbamate

Guidance literature:: Multi-step reaction with 5 steps

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

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

3.1: boron tribromide / dichloromethane / 0.67 h / 0 °C

3.2: 0.5 h

4.1: sodium tris(acetoxy)borohydride / 1,2-dichloro-ethane / 6 h / 20 °C

5.1: triethylamine / methanol / 2 h / 50 °C

With 1,10-Phenanthroline; boron tribromide; sodium tris(acetoxy)borohydride; caesium carbonate; triethylamine; hydrazine; copper(l) iodide; In methanol; ethanol; dichloromethane; 1,2-dichloro-ethane;