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N-tert-butyl ester-N-(4-benzylsulfanyl-5-nitro-thiophen-3-ylmethyl)-methanesulfonamide

Base Information
  • Chemical Name:N-tert-butyl ester-N-(4-benzylsulfanyl-5-nitro-thiophen-3-ylmethyl)-methanesulfonamide
  • CAS No.:1002761-80-9
  • Molecular Formula:C18H22N2O6S3
  • Molecular Weight:458.58
  • Hs Code.:
N-tert-butyl ester-N-(4-benzylsulfanyl-5-nitro-thiophen-3-ylmethyl)-methanesulfonamide

Synonyms:N-tert-butyl ester-N-(4-benzylsulfanyl-5-nitro-thiophen-3-ylmethyl)-methanesulfonamide

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Chemical Property of N-tert-butyl ester-N-(4-benzylsulfanyl-5-nitro-thiophen-3-ylmethyl)-methanesulfonamide
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Technology Process of N-tert-butyl ester-N-(4-benzylsulfanyl-5-nitro-thiophen-3-ylmethyl)-methanesulfonamide

There total 7 articles about N-tert-butyl ester-N-(4-benzylsulfanyl-5-nitro-thiophen-3-ylmethyl)-methanesulfonamide 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:
With potassium carbonate; In N,N-dimethyl acetamide; at 55 ℃; for 16h; Product distribution / selectivity;
Guidance literature:
With diethylazodicarboxylate; trimethylphosphane; In tetrahydrofuran; toluene; at 25 ℃; for 3.5h;
Guidance literature:
Multi-step reaction with 2 steps
1.1: diisobutylaluminium hydride / dichloromethane / 0.25 h / -40 °C
1.2: 1 h / 25 °C
2.1: trimethylphosphane / tetrahydrofuran / 0.42 h / 25 °C
2.2: 25 °C
With diisobutylaluminium hydride; trimethylphosphane; In tetrahydrofuran; dichloromethane;
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