C₁₉H₂₀F₂N₄O₃S*ClH

Base Information

Chemical Name:C₁₉H₂₀F₂N₄O₃S*ClH
CAS No.:1403467-62-8
Molecular Formula:C₁₉H₂₀F₂N₄O₃S*ClH
Molecular Weight:458.917
Hs Code.:

C<sub>19</sub>H<sub>20</sub>F<sub>2</sub>N<sub>4</sub>O<sub>3</sub>S*ClH

Synonyms:C₁₉H₂₀F₂N₄O₃S*ClH

Suppliers and Price of C₁₉H₂₀F₂N₄O₃S*ClH

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemicals and raw materials
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Total 1 raw suppliers

Chemical Property of C₁₉H₂₀F₂N₄O₃S*ClH

Chemical Property:

Purity/Quality:: 98% ^*data from raw suppliers

Safty Information:

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Technology Process of C₁₉H₂₀F₂N₄O₃S*ClH

There total 7 articles about C₁₉H₂₀F₂N₄O₃S*ClH 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: 81.0%

: 1403467-66-2
C₁₉H₂₀F₂N₄O₃S*ClH

: 1403467-62-8
C₁₉H₂₀F₂N₄O₃S*ClH

Guidance literature:: C₁₉H₂₀F₂N₄O₃S*ClH; With copper(l) chloride; In ethanol; for 4h; Reflux;

With hydrogenchloride; In diethyl ether;

Reference yield:

: 14668-29-2
2-methyl-2-(methylsulfonyl)propanenitrile

: 1403467-62-8
C₁₉H₂₀F₂N₄O₃S*ClH

Guidance literature:: Multi-step reaction with 5 steps

1.1: n-butyllithium / tetrahydrofuran; hexanes / 0.5 h / -78 °C

1.2: 2 h / -78 °C

2.1: hydrogenchloride / 1,4-dioxane; methanol / 1.5 h / 25 °C

3.1: hydrogen / palladium 10% on activated carbon / methanol / 4 h / 25 °C

4.1: bis-(2-oxo-3-oxazolidinyl)phosphoryl chloride; N-ethyl-N,N-diisopropylamine / dichloromethane / 0.67 h / 25 °C

5.1: copper(l) chloride / ethanol / 4 h / Reflux

With hydrogenchloride; n-butyllithium; hydrogen; bis-(2-oxo-3-oxazolidinyl)phosphoryl chloride; N-ethyl-N,N-diisopropylamine; copper(l) chloride; palladium 10% on activated carbon; In tetrahydrofuran; 1,4-dioxane; methanol; hexanes; ethanol; dichloromethane;

Reference yield:

: 445-27-2
2'-Fluoroacetophenone

: 1403467-62-8
C₁₉H₂₀F₂N₄O₃S*ClH

Guidance literature:: Multi-step reaction with 7 steps

1.1: nitric acid; sulfuric acid / 0.5 h / -42 °C

2.1: titanium(IV) tetraethanolate / tetrahydrofuran / 20 h / Reflux

3.1: n-butyllithium / tetrahydrofuran; hexanes / 0.5 h / -78 °C

3.2: 2 h / -78 °C

4.1: hydrogenchloride / 1,4-dioxane; methanol / 1.5 h / 25 °C

5.1: hydrogen / palladium 10% on activated carbon / methanol / 4 h / 25 °C

6.1: bis-(2-oxo-3-oxazolidinyl)phosphoryl chloride; N-ethyl-N,N-diisopropylamine / dichloromethane / 0.67 h / 25 °C

7.1: copper(l) chloride / ethanol / 4 h / Reflux

With hydrogenchloride; titanium(IV) tetraethanolate; n-butyllithium; sulfuric acid; hydrogen; nitric acid; bis-(2-oxo-3-oxazolidinyl)phosphoryl chloride; N-ethyl-N,N-diisopropylamine; copper(l) chloride; palladium 10% on activated carbon; In tetrahydrofuran; 1,4-dioxane; methanol; hexanes; ethanol; dichloromethane;