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3-[1-(cyclohexylacetyl)piperidin-4-yl]-7-[4-(methylsulfonyl)phenyl]-3,4-dihydro-2H-1,4-benzoxazine trifluoroacetate

Base Information
  • Chemical Name:3-[1-(cyclohexylacetyl)piperidin-4-yl]-7-[4-(methylsulfonyl)phenyl]-3,4-dihydro-2H-1,4-benzoxazine trifluoroacetate
  • CAS No.:1200575-40-1
  • Molecular Formula:C2HF3O2*C28H36N2O4S
  • Molecular Weight:610.695
  • Hs Code.:
3-[1-(cyclohexylacetyl)piperidin-4-yl]-7-[4-(methylsulfonyl)phenyl]-3,4-dihydro-2H-1,4-benzoxazine trifluoroacetate

Synonyms:3-[1-(cyclohexylacetyl)piperidin-4-yl]-7-[4-(methylsulfonyl)phenyl]-3,4-dihydro-2H-1,4-benzoxazine trifluoroacetate

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Chemical Property of 3-[1-(cyclohexylacetyl)piperidin-4-yl]-7-[4-(methylsulfonyl)phenyl]-3,4-dihydro-2H-1,4-benzoxazine trifluoroacetate
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Technology Process of 3-[1-(cyclohexylacetyl)piperidin-4-yl]-7-[4-(methylsulfonyl)phenyl]-3,4-dihydro-2H-1,4-benzoxazine trifluoroacetate

There total 11 articles about 3-[1-(cyclohexylacetyl)piperidin-4-yl]-7-[4-(methylsulfonyl)phenyl]-3,4-dihydro-2H-1,4-benzoxazine trifluoroacetate 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:
7-[4-(methylsulfonyl)phenyl]-3-piperidin-4-yl-3,4-dihydro-2H-1,4-benzoxazine.; Cyclohexylacetic acid; With O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; triethylamine; In N,N-dimethyl-formamide; at 20 ℃;
trifluoroacetic acid; In water; acetonitrile;
Guidance literature:
Multi-step reaction with 4 steps
1: sodium tetrahydroborate / ethanol / 6 h
2: sodium hydrogencarbonate; triphenylphosphine / palladium diacetate / ethanol / 80 °C
3: dichloromethane / 0.5 h
4: O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; triethylamine / N,N-dimethyl-formamide / 20 °C
With sodium tetrahydroborate; sodium hydrogencarbonate; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; triethylamine; triphenylphosphine; palladium diacetate; In ethanol; dichloromethane; N,N-dimethyl-formamide;
Guidance literature:
Multi-step reaction with 7 steps
1.1: water; hydrogen bromide; sodium nitrite / 0.17 h / 0 °C
1.2: 0 °C
2.1: hydrogenchloride; water / ethanol / 3 h / 100 °C
3.1: potassium carbonate / N,N-dimethyl-formamide / 0.75 h
3.2: 20 °C
4.1: sodium tetrahydroborate / ethanol / 6 h
5.1: sodium hydrogencarbonate; triphenylphosphine / palladium diacetate / ethanol / 80 °C
6.1: dichloromethane / 0.5 h
7.1: O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; triethylamine / N,N-dimethyl-formamide / 20 °C
With hydrogenchloride; sodium tetrahydroborate; water; hydrogen bromide; sodium hydrogencarbonate; potassium carbonate; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; triethylamine; triphenylphosphine; sodium nitrite; palladium diacetate; In ethanol; dichloromethane; N,N-dimethyl-formamide;
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