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4-{2'-fluoro-4'-[1-oxo-1-(3-(1,2,3,4-tetrahydroacridin-9-ylamino)propylamino)propan-2-yl]biphenyl-4-yloxy}butyl nitrate

Base Information
  • Chemical Name:4-{2'-fluoro-4'-[1-oxo-1-(3-(1,2,3,4-tetrahydroacridin-9-ylamino)propylamino)propan-2-yl]biphenyl-4-yloxy}butyl nitrate
  • CAS No.:1435359-89-9
  • Molecular Formula:C35H39FN4O5
  • Molecular Weight:614.717
  • Hs Code.:
4-{2'-fluoro-4'-[1-oxo-1-(3-(1,2,3,4-tetrahydroacridin-9-ylamino)propylamino)propan-2-yl]biphenyl-4-yloxy}butyl nitrate

Synonyms:4-{2'-fluoro-4'-[1-oxo-1-(3-(1,2,3,4-tetrahydroacridin-9-ylamino)propylamino)propan-2-yl]biphenyl-4-yloxy}butyl nitrate

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Chemical Property of 4-{2'-fluoro-4'-[1-oxo-1-(3-(1,2,3,4-tetrahydroacridin-9-ylamino)propylamino)propan-2-yl]biphenyl-4-yloxy}butyl nitrate
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Technology Process of 4-{2'-fluoro-4'-[1-oxo-1-(3-(1,2,3,4-tetrahydroacridin-9-ylamino)propylamino)propan-2-yl]biphenyl-4-yloxy}butyl nitrate

There total 12 articles about 4-{2'-fluoro-4'-[1-oxo-1-(3-(1,2,3,4-tetrahydroacridin-9-ylamino)propylamino)propan-2-yl]biphenyl-4-yloxy}butyl nitrate 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:
2-{2-fluoro-4'-[4-(nitrooxy)butoxy]biphenyl-4-yl}propanoic acid; With dicyclohexyl-carbodiimide; In dichloromethane; at 20 ℃; for 0.5h;
N-(1,2,3,4-tetrahydroacridin-9-yl)propane-1,3-diamine; With dmap; In dichloromethane; at 20 ℃; for 24h;
DOI:10.1016/j.bmcl.2013.04.008
Guidance literature:
Multi-step reaction with 3 steps
1.1: trichlorophosphate / 3 h / Reflux
2.1: pentan-1-ol / 18 h / Inert atmosphere; Reflux
3.1: dicyclohexyl-carbodiimide / dichloromethane / 0.5 h / 20 °C
3.2: 24 h / 20 °C
With dicyclohexyl-carbodiimide; trichlorophosphate; In dichloromethane; pentan-1-ol; 1.1: |Friedel-Crafts Alkylation;
DOI:10.1016/j.bmcl.2013.04.008
Guidance literature:
Multi-step reaction with 3 steps
1.1: trichlorophosphate / 3 h / Reflux
2.1: pentan-1-ol / 18 h / Inert atmosphere; Reflux
3.1: dicyclohexyl-carbodiimide / dichloromethane / 0.5 h / 20 °C
3.2: 24 h / 20 °C
With dicyclohexyl-carbodiimide; trichlorophosphate; In dichloromethane; pentan-1-ol; 1.1: |Friedel-Crafts Alkylation;
DOI:10.1016/j.bmcl.2013.04.008
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