{6-(4-Chloro-phenyl)-2-oxo-1-[(3,3,3-trifluoro-2-hydroxy-1-isopropyl-propylcarbamoyl)-methyl]-1,2-dihydro-pyridin-3-yl}-carbamic acid benzyl ester

Base Information

Chemical Name:{6-(4-Chloro-phenyl)-2-oxo-1-[(3,3,3-trifluoro-2-hydroxy-1-isopropyl-propylcarbamoyl)-methyl]-1,2-dihydro-pyridin-3-yl}-carbamic acid benzyl ester
CAS No.:147283-30-5
Molecular Formula:C₂₇H₂₇ClF₃N₃O₅
Molecular Weight:565.977
Hs Code.:

{6-(4-Chloro-phenyl)-2-oxo-1-[(3,3,3-trifluoro-2-hydroxy-1-isopropyl-propylcarbamoyl)-methyl]-1,2-dihydro-pyridin-3-yl}-carbamic acid benzyl ester

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Chemical Property of {6-(4-Chloro-phenyl)-2-oxo-1-[(3,3,3-trifluoro-2-hydroxy-1-isopropyl-propylcarbamoyl)-methyl]-1,2-dihydro-pyridin-3-yl}-carbamic acid benzyl ester

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Technology Process of {6-(4-Chloro-phenyl)-2-oxo-1-[(3,3,3-trifluoro-2-hydroxy-1-isopropyl-propylcarbamoyl)-methyl]-1,2-dihydro-pyridin-3-yl}-carbamic acid benzyl ester

There total 10 articles about {6-(4-Chloro-phenyl)-2-oxo-1-[(3,3,3-trifluoro-2-hydroxy-1-isopropyl-propylcarbamoyl)-methyl]-1,2-dihydro-pyridin-3-yl}-carbamic acid benzyl ester 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:

: 147269-30-5
[1-{[2-(tert-Butyl-dimethyl-silanyloxy)-3,3,3-trifluoro-1-isopropyl-propylcarbamoyl]-methyl}-6-(4-chloro-phenyl)-2-oxo-1,2-dihydro-pyridin-3-yl]-carbamic acid benzyl ester

: 147283-30-5
{6-(4-Chloro-phenyl)-2-oxo-1-[(3,3,3-trifluoro-2-hydroxy-1-isopropyl-propylcarbamoyl)-methyl]-1,2-dihydro-pyridin-3-yl}-carbamic acid benzyl ester

Guidance literature:: With tetrabutyl ammonium fluoride; In tetrahydrofuran;
DOI:10.1021/jm00046a015

Reference yield:

: 106746-09-2
3(RS)-amino-1,1,1-trifluoro-2(RS)-hydroxy-4-methylpentane hydrochloride

: 147283-30-5
{6-(4-Chloro-phenyl)-2-oxo-1-[(3,3,3-trifluoro-2-hydroxy-1-isopropyl-propylcarbamoyl)-methyl]-1,2-dihydro-pyridin-3-yl}-carbamic acid benzyl ester

Guidance literature:: Multi-step reaction with 5 steps

1: 4-methyl-morpholine / tetrahydrofuran / 12 h

2: 2,6-dimethylpyridine / dichloromethane / 12 h

3: sodium iodide / acetone / 12 h / Ambient temperature

4: sodium hydride / 1.) DMF, RT, 2.) DMF, RT

5: tetrabutyl ammonium fluoride / tetrahydrofuran

With 4-methyl-morpholine; 2,6-dimethylpyridine; tetrabutyl ammonium fluoride; sodium hydride; sodium iodide; In tetrahydrofuran; dichloromethane; acetone;
DOI:10.1021/jm00046a015

Reference yield:

: 23148-51-8
3-cyano-6-(4-chlorophenyl)pyridine-2(1H)-one

: 147283-30-5
{6-(4-Chloro-phenyl)-2-oxo-1-[(3,3,3-trifluoro-2-hydroxy-1-isopropyl-propylcarbamoyl)-methyl]-1,2-dihydro-pyridin-3-yl}-carbamic acid benzyl ester

Guidance literature:: Multi-step reaction with 5 steps

1: hydrogen bromide / acetic acid / Heating

2: diphenyl-phosphinic acid; triethylamine / 1,4-dioxane / Heating

3: 1,4-dioxane / Heating

4: sodium hydride / 1.) DMF, RT, 2.) DMF, RT

5: tetrabutyl ammonium fluoride / tetrahydrofuran

With diphenyl-phosphinic acid; tetrabutyl ammonium fluoride; hydrogen bromide; sodium hydride; triethylamine; In tetrahydrofuran; 1,4-dioxane; acetic acid;
DOI:10.1021/jm00046a015