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N-{2'-[5-(3-chloro-4-methylphenylamino)-1,2,4-thiadiazol-3-yl]-1'-methylethyl}-(2'',2'',6'',6''-tetramethylpiperidin-4''-yl)aminodocosa-4Z,7Z,10Z,13Z,16Z,19Z-hexaenoic acid amide

Base Information
  • Chemical Name:N-{2'-[5-(3-chloro-4-methylphenylamino)-1,2,4-thiadiazol-3-yl]-1'-methylethyl}-(2'',2'',6'',6''-tetramethylpiperidin-4''-yl)aminodocosa-4Z,7Z,10Z,13Z,16Z,19Z-hexaenoic acid amide
  • CAS No.:1421276-58-5
  • Molecular Formula:C43H62ClN5OS
  • Molecular Weight:732.517
  • Hs Code.:
N-{2'-[5-(3-chloro-4-methylphenylamino)-1,2,4-thiadiazol-3-yl]-1'-methylethyl}-(2'',2'',6'',6''-tetramethylpiperidin-4''-yl)aminodocosa-4Z,7Z,10Z,13Z,16Z,19Z-hexaenoic acid amide

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Chemical Property of N-{2'-[5-(3-chloro-4-methylphenylamino)-1,2,4-thiadiazol-3-yl]-1'-methylethyl}-(2'',2'',6'',6''-tetramethylpiperidin-4''-yl)aminodocosa-4Z,7Z,10Z,13Z,16Z,19Z-hexaenoic acid amide
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Technology Process of N-{2'-[5-(3-chloro-4-methylphenylamino)-1,2,4-thiadiazol-3-yl]-1'-methylethyl}-(2'',2'',6'',6''-tetramethylpiperidin-4''-yl)aminodocosa-4Z,7Z,10Z,13Z,16Z,19Z-hexaenoic acid amide

There total 3 articles about N-{2'-[5-(3-chloro-4-methylphenylamino)-1,2,4-thiadiazol-3-yl]-1'-methylethyl}-(2'',2'',6'',6''-tetramethylpiperidin-4''-yl)aminodocosa-4Z,7Z,10Z,13Z,16Z,19Z-hexaenoic acid 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:
docosahexaenoic acid; With triethylamine; isobutyl chloroformate; In acetonitrile; at 0 - 4 ℃; for 0.333333h; Inert atmosphere;
N-{2-[5-(4-methyl-3-chlorophenylamino)-[1,2,4]thiadiazol-3-yl]-1-methylethyl}-(2,2,6,6-tetramethylpiperidine-4-yl)-amine; In methanol; acetonitrile; at 20 ℃; for 1h; Inert atmosphere;
DOI:10.1134/S0012500812110031
Guidance literature:
Multi-step reaction with 3 steps
1.1: methanol / 20 °C
2.1: sodium tetrahydroborate / methanol / 2 h / 40 - 50 °C
3.1: triethylamine; isobutyl chloroformate / acetonitrile / 0.33 h / 0 - 4 °C / Inert atmosphere
3.2: 1 h / 20 °C / Inert atmosphere
With sodium tetrahydroborate; triethylamine; isobutyl chloroformate; In methanol; acetonitrile;
DOI:10.1134/S0012500812110031
Guidance literature:
Multi-step reaction with 3 steps
1.1: methanol / 20 °C
2.1: sodium tetrahydroborate / methanol / 2 h / 40 - 50 °C
3.1: triethylamine; isobutyl chloroformate / acetonitrile / 0.33 h / 0 - 4 °C / Inert atmosphere
3.2: 1 h / 20 °C / Inert atmosphere
With sodium tetrahydroborate; triethylamine; isobutyl chloroformate; In methanol; acetonitrile;
DOI:10.1134/S0012500812110031
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