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C21H31BrN2O4

Base Information
  • Chemical Name:C21H31BrN2O4
  • CAS No.:1393110-64-9
  • Molecular Formula:C21H31BrN2O4
  • Molecular Weight:455.392
  • Hs Code.:
C<sub>21</sub>H<sub>31</sub>BrN<sub>2</sub>O<sub>4</sub>

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Chemical Property of C21H31BrN2O4
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Technology Process of C21H31BrN2O4

There total 8 articles about C21H31BrN2O4 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:
Multi-step reaction with 5 steps
1: silver carbonate / chloroform / 60 h
2: DBDMH / tetrahydrofuran / 72 h
3: N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile) / tetrachloromethane / Reflux
4: 1,3-dimethyl-3,4,5,6-tetrahydro-2(1H)-pyrimidinone; lithium diisopropyl amide / tetrahydrofuran / -50 - 10 °C
5: diethyl ether
With 1,3-dimethyl-3,4,5,6-tetrahydro-2(1H)-pyrimidinone; N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile); silver carbonate; lithium diisopropyl amide; In tetrahydrofuran; tetrachloromethane; diethyl ether; chloroform;
DOI:10.1007/s11426-011-4480-y
Guidance literature:
Multi-step reaction with 4 steps
1: DBDMH / tetrahydrofuran / 72 h
2: N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile) / tetrachloromethane / Reflux
3: 1,3-dimethyl-3,4,5,6-tetrahydro-2(1H)-pyrimidinone; lithium diisopropyl amide / tetrahydrofuran / -50 - 10 °C
4: diethyl ether
With 1,3-dimethyl-3,4,5,6-tetrahydro-2(1H)-pyrimidinone; N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile); lithium diisopropyl amide; In tetrahydrofuran; tetrachloromethane; diethyl ether;
DOI:10.1007/s11426-011-4480-y
Guidance literature:
Multi-step reaction with 3 steps
1: tris-(dibenzylideneacetone)dipalladium(0); caesium carbonate; tert-butyl XPhos / toluene / 5 h / 80 °C
2: 1,3-dimethyl-3,4,5,6-tetrahydro-2(1H)-pyrimidinone; lithium diisopropyl amide / tetrahydrofuran / -50 - 10 °C
3: diethyl ether
With 1,3-dimethyl-3,4,5,6-tetrahydro-2(1H)-pyrimidinone; tris-(dibenzylideneacetone)dipalladium(0); caesium carbonate; lithium diisopropyl amide; tert-butyl XPhos; In tetrahydrofuran; diethyl ether; toluene; 1: Buchwald-Hartwig coupling;
DOI:10.1007/s11426-011-4480-y
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