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(S,S)-2-methyl-2-propanesulfinic acid [1-(3-cyclopropylmethoxy-4-difluoromethoxyphenyl)-2-(pyridin-4-yl)ethyl]amide

Base Information
  • Chemical Name:(S,S)-2-methyl-2-propanesulfinic acid [1-(3-cyclopropylmethoxy-4-difluoromethoxyphenyl)-2-(pyridin-4-yl)ethyl]amide
  • CAS No.:1367625-82-8
  • Molecular Formula:C22H28F2N2O3S
  • Molecular Weight:438.539
  • Hs Code.:
(S,S)-2-methyl-2-propanesulfinic acid [1-(3-cyclopropylmethoxy-4-difluoromethoxyphenyl)-2-(pyridin-4-yl)ethyl]amide

Synonyms:(S,S)-2-methyl-2-propanesulfinic acid [1-(3-cyclopropylmethoxy-4-difluoromethoxyphenyl)-2-(pyridin-4-yl)ethyl]amide

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Chemical Property of (S,S)-2-methyl-2-propanesulfinic acid [1-(3-cyclopropylmethoxy-4-difluoromethoxyphenyl)-2-(pyridin-4-yl)ethyl]amide
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Technology Process of (S,S)-2-methyl-2-propanesulfinic acid [1-(3-cyclopropylmethoxy-4-difluoromethoxyphenyl)-2-(pyridin-4-yl)ethyl]amide

There total 2 articles about (S,S)-2-methyl-2-propanesulfinic acid [1-(3-cyclopropylmethoxy-4-difluoromethoxyphenyl)-2-(pyridin-4-yl)ethyl]amide 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:
picoline; With n-butyllithium; In tetrahydrofuran; at -78 - 0 ℃; for 0.5h;
(S)-2-methyl-2-propanesulfinic acid 3-cyclopropylmethoxy-4-(difluoromethoxy)benzylideneamide; In tetrahydrofuran; at -78 ℃; for 3h; optical yield given as %de;
DOI:10.1039/c2ob06495b
Guidance literature:
Multi-step reaction with 2 steps
1.1: titanium(IV) tetraethanolate / tetrahydrofuran / 12 h / 20 °C
2.1: n-butyllithium / tetrahydrofuran / 0.5 h / -78 - 0 °C
2.2: 3 h / -78 °C
With titanium(IV) tetraethanolate; n-butyllithium; In tetrahydrofuran;
DOI:10.1039/c2ob06495b
Guidance literature:
Multi-step reaction with 3 steps
1.1: hydrogenchloride / 1,4-dioxane; water / 0 - 20 °C
2.1: ethanol / 12 h / Reflux
3.1: sodium hydride / N,N-dimethyl-formamide / 1 h / 0 °C
3.2: 3.17 h / 0 °C / Heating
With hydrogenchloride; sodium hydride; In 1,4-dioxane; ethanol; water; N,N-dimethyl-formamide;
DOI:10.1039/c2ob06495b
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