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N-(6-{[(2R,3S)-3,4-dihydroxy-2-butanyl]oxy}-2-[(4-fluorobenzyl)sulfanyl]-4-pyrimidinyl)-3-methyl-1-azetidinesulfonamide

Base Information Edit
  • Chemical Name:N-(6-{[(2R,3S)-3,4-dihydroxy-2-butanyl]oxy}-2-[(4-fluorobenzyl)sulfanyl]-4-pyrimidinyl)-3-methyl-1-azetidinesulfonamide
  • CAS No.:1418112-77-2
  • Molecular Formula:C19H25FN4O5S2
  • Molecular Weight:472.562
  • Hs Code.:
  • Mol file:1418112-77-2.mol
N-(6-{[(2R,3S)-3,4-dihydroxy-2-butanyl]oxy}-2-[(4-fluorobenzyl)sulfanyl]-4-pyrimidinyl)-3-methyl-1-azetidinesulfonamide

Synonyms:N-(6-{[(2R,3S)-3,4-dihydroxy-2-butanyl]oxy}-2-[(4-fluorobenzyl)sulfanyl]-4-pyrimidinyl)-3-methyl-1-azetidinesulfonamide

Suppliers and Price of N-(6-{[(2R,3S)-3,4-dihydroxy-2-butanyl]oxy}-2-[(4-fluorobenzyl)sulfanyl]-4-pyrimidinyl)-3-methyl-1-azetidinesulfonamide
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
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Total 2 raw suppliers
Chemical Property of N-(6-{[(2R,3S)-3,4-dihydroxy-2-butanyl]oxy}-2-[(4-fluorobenzyl)sulfanyl]-4-pyrimidinyl)-3-methyl-1-azetidinesulfonamide Edit
Chemical Property:
Purity/Quality:

97% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
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Technology Process of N-(6-{[(2R,3S)-3,4-dihydroxy-2-butanyl]oxy}-2-[(4-fluorobenzyl)sulfanyl]-4-pyrimidinyl)-3-methyl-1-azetidinesulfonamide

There total 6 articles about N-(6-{[(2R,3S)-3,4-dihydroxy-2-butanyl]oxy}-2-[(4-fluorobenzyl)sulfanyl]-4-pyrimidinyl)-3-methyl-1-azetidinesulfonamide 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:
Guidance literature:
N-(6-((R)-1-((S)-2,2-dimethyl-1,3-dioxolan-4-yl)ethoxy)-2-(4-fluorobenzyl-thio)pyrimidin-4-yl)-3-methylazetidine-1-sulfonamide; With trifluoroacetic acid; In dichloromethane; at 0 - 20 ℃; for 18h;
With ammonia; In methanol; for 0.333333h;
Guidance literature:
Multi-step reaction with 4 steps
1.1: trichlorophosphate; N-benzyl-N,N,N-triethylammonium chloride / 1,2-dimethoxyethane / 10 h / Reflux
2.1: sodium hydride / tetrahydrofuran; 2-methyltetrahydrofuran; mineral oil / 20.33 h / 0 - 20 °C
3.1: XPhos; tris-(dibenzylideneacetone)dipalladium(0); potassium carbonate / 1,4-dioxane / 1 h / 100 °C / Inert atmosphere
4.1: trifluoroacetic acid / dichloromethane / 18 h / 0 - 20 °C
4.2: 0.33 h
With tris-(dibenzylideneacetone)dipalladium(0); N-benzyl-N,N,N-triethylammonium chloride; sodium hydride; potassium carbonate; trifluoroacetic acid; XPhos; trichlorophosphate; In tetrahydrofuran; 2-methyltetrahydrofuran; 1,4-dioxane; 1,2-dimethoxyethane; dichloromethane; mineral oil;
Guidance literature:
Multi-step reaction with 5 steps
1.1: sodium acetate / acetonitrile; water / 22 h / 20 °C
2.1: trichlorophosphate; N-benzyl-N,N,N-triethylammonium chloride / 1,2-dimethoxyethane / 10 h / Reflux
3.1: sodium hydride / tetrahydrofuran; 2-methyltetrahydrofuran; mineral oil / 20.33 h / 0 - 20 °C
4.1: XPhos; tris-(dibenzylideneacetone)dipalladium(0); potassium carbonate / 1,4-dioxane / 1 h / 100 °C / Inert atmosphere
5.1: trifluoroacetic acid / dichloromethane / 18 h / 0 - 20 °C
5.2: 0.33 h
With tris-(dibenzylideneacetone)dipalladium(0); N-benzyl-N,N,N-triethylammonium chloride; sodium acetate; sodium hydride; potassium carbonate; trifluoroacetic acid; XPhos; trichlorophosphate; In tetrahydrofuran; 2-methyltetrahydrofuran; 1,4-dioxane; 1,2-dimethoxyethane; dichloromethane; water; acetonitrile; mineral oil;
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