N-((2R,3R)-3-allyloxy-4-(4-fluoro-N-methylphenylsulfonamido)-2-methylbutyl)-N-((S)-1-((4-methoxybenzyl)oxy)propan-2-yl)-1-methyl-5-((S)-pent-4-en-2yloxy)-1H-pyrazole-4-carboxamide

Base Information

Chemical Name:N-((2R,3R)-3-allyloxy-4-(4-fluoro-N-methylphenylsulfonamido)-2-methylbutyl)-N-((S)-1-((4-methoxybenzyl)oxy)propan-2-yl)-1-methyl-5-((S)-pent-4-en-2yloxy)-1H-pyrazole-4-carboxamide
CAS No.:1403480-83-0
Molecular Formula:C₃₆H₄₉FN₄O₇S
Molecular Weight:700.872
Hs Code.:

N-((2R,3R)-3-allyloxy-4-(4-fluoro-N-methylphenylsulfonamido)-2-methylbutyl)-N-((S)-1-((4-methoxybenzyl)oxy)propan-2-yl)-1-methyl-5-((S)-pent-4-en-2yloxy)-1H-pyrazole-4-carboxamide

Synonyms:

Suppliers and Price of N-((2R,3R)-3-allyloxy-4-(4-fluoro-N-methylphenylsulfonamido)-2-methylbutyl)-N-((S)-1-((4-methoxybenzyl)oxy)propan-2-yl)-1-methyl-5-((S)-pent-4-en-2yloxy)-1H-pyrazole-4-carboxamide

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 N-((2R,3R)-3-allyloxy-4-(4-fluoro-N-methylphenylsulfonamido)-2-methylbutyl)-N-((S)-1-((4-methoxybenzyl)oxy)propan-2-yl)-1-methyl-5-((S)-pent-4-en-2yloxy)-1H-pyrazole-4-carboxamide

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of N-((2R,3R)-3-allyloxy-4-(4-fluoro-N-methylphenylsulfonamido)-2-methylbutyl)-N-((S)-1-((4-methoxybenzyl)oxy)propan-2-yl)-1-methyl-5-((S)-pent-4-en-2yloxy)-1H-pyrazole-4-carboxamide

There total 9 articles about N-((2R,3R)-3-allyloxy-4-(4-fluoro-N-methylphenylsulfonamido)-2-methylbutyl)-N-((S)-1-((4-methoxybenzyl)oxy)propan-2-yl)-1-methyl-5-((S)-pent-4-en-2yloxy)-1H-pyrazole-4-carboxamide 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:

: 1403480-62-5
N-((2R,3R)-4-(4-fluoro-N-methylphenylsulfonamido)-3-hydroxy-2-methylbutyl)-N-((S)-1-((4-methoxybenzyl)oxy)propan-2-yl)-1-methyl-5-((S)-pent-4-en-2yloxy)-1H-pyrazole-4-carboxamide

: 106-95-6
allyl bromide

: 1403480-83-0
N-((2R,3R)-3-allyloxy-4-(4-fluoro-N-methylphenylsulfonamido)-2-methylbutyl)-N-((S)-1-((4-methoxybenzyl)oxy)propan-2-yl)-1-methyl-5-((S)-pent-4-en-2yloxy)-1H-pyrazole-4-carboxamide

Guidance literature:: With sodium hydride; In N,N-dimethyl-formamide; at 0 - 20 ℃;
DOI:10.1021/jm500994n

Reference yield:

: 1255212-77-1
tert-butyl ((2R,3S)-2-((tert-butyldimethylsilyl)oxy)-4-(((2S)-1-((4-methoxybenzyl)oxy)propan-2-yl)amino)-3-methyl-4-oxobutyl)(methyl)carbamate

: 1403480-83-0
N-((2R,3R)-3-allyloxy-4-(4-fluoro-N-methylphenylsulfonamido)-2-methylbutyl)-N-((S)-1-((4-methoxybenzyl)oxy)propan-2-yl)-1-methyl-5-((S)-pent-4-en-2yloxy)-1H-pyrazole-4-carboxamide

Guidance literature:: Multi-step reaction with 7 steps

1: 2,6-dimethylpyridine / dichloromethane / 3.92 h / 0 - 20 °C / Inert atmosphere

2: potassium carbonate / tetrahydrofuran; methanol; water / 3 h / 20 °C

3: 2,6-dimethylpyridine / dichloromethane / 18 h / 20 °C

4: dimethylsulfide borane complex / tetrahydrofuran / 6.25 h / 0 - 65 °C / Inert atmosphere

5: N-ethyl-N,N-diisopropylamine; bis-(2-oxo-3-oxazolidinyl)phosphoryl chloride / dichloromethane / 0 - 20 °C

6: tetrabutyl ammonium fluoride / tetrahydrofuran / 20 °C

7: sodium hydride / N,N-dimethyl-formamide / 0 - 20 °C

With 2,6-dimethylpyridine; dimethylsulfide borane complex; tetrabutyl ammonium fluoride; bis-(2-oxo-3-oxazolidinyl)phosphoryl chloride; sodium hydride; potassium carbonate; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; methanol; dichloromethane; water; N,N-dimethyl-formamide;
DOI:10.1021/jm500994n

Reference yield:

: C₃₀H₅₆N₂O₆Si₂

: 1403480-83-0
N-((2R,3R)-3-allyloxy-4-(4-fluoro-N-methylphenylsulfonamido)-2-methylbutyl)-N-((S)-1-((4-methoxybenzyl)oxy)propan-2-yl)-1-methyl-5-((S)-pent-4-en-2yloxy)-1H-pyrazole-4-carboxamide

Guidance literature:: Multi-step reaction with 6 steps

1: potassium carbonate / tetrahydrofuran; methanol; water / 3 h / 20 °C

2: 2,6-dimethylpyridine / dichloromethane / 18 h / 20 °C

3: dimethylsulfide borane complex / tetrahydrofuran / 6.25 h / 0 - 65 °C / Inert atmosphere

4: N-ethyl-N,N-diisopropylamine; bis-(2-oxo-3-oxazolidinyl)phosphoryl chloride / dichloromethane / 0 - 20 °C

5: tetrabutyl ammonium fluoride / tetrahydrofuran / 20 °C

6: sodium hydride / N,N-dimethyl-formamide / 0 - 20 °C

With 2,6-dimethylpyridine; dimethylsulfide borane complex; tetrabutyl ammonium fluoride; bis-(2-oxo-3-oxazolidinyl)phosphoryl chloride; sodium hydride; potassium carbonate; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; methanol; dichloromethane; water; N,N-dimethyl-formamide;
DOI:10.1021/jm500994n