3-(4-fluorophenoxy)propyl bromide

CC#C[C@H](C)Oc1cc(N)c(Cl)cc1C(=O)N[C@H]1CCN(CCCOc2ccc(F)cc2)C[C@H]1OC
Reaction #1031
title compound
Rendimiento 91.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)(C)OC(=O)N1CCC(c2ccc(OCCCOc3ccc(F)cc3)cc2)C(O)C1
Reaction #197768
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
[Br-]
Reaction #264517
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CC#C[C@H](C)Oc1cc(N)c(Cl)cc1C(=O)N[C@H]1CCN(CCCOc2ccc(F)cc2)C[C@H]1OC
Reaction #430607
title compound
Rendimiento 91.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_01
Br.Cc1ccc2c(c1)n(Cc1ccc(Br)cc1)c(=N)n2CCCOc1ccc(F)cc1
Reaction #497538
3-(4-bromo-benzyl)-1-[3-(4-fluoro-phenoxy)-propyl]-5-methyl-1,3-dihydrobenzoimidazol-2-ylideneamine, hydrobromide salt
Rendimiento 33.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_06
OCCc1cccc(OCCCOc2ccc(F)cc2)c1
Reaction #554526
title compound
Rendimiento 95.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1992_10
OC(c1ccccc1)(c1ccccc1)C12CC[N+](CCCOc3ccc(F)cc3)(CC1)CC2.[Br-]
Reaction #621030
desired product
Rendimiento 43.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_10
CC(C)(C)OC(=O)N1CCC(c2ccc(OCCCOc3ccc(F)cc3)cc2)C(O)C1
Reaction #1263660
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_11
OCCc1cccc(OCCCOc2ccc(F)cc2)c1
Reaction #1675608
title compound
Rendimiento 95.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_06
OC(c1ccccc1)(c1ccccc1)C12CC[N+](CCCOc3ccc(F)cc3)(CC1)CC2.[Br-]
Reaction #1812140
desired product
Rendimiento 43.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_02
OC(c1ccccc1)(c1ccccc1)C12CC[N+](CCCOc3ccc(F)cc3)(CC1)CC2.[Br-]
Reaction #1869674
desired product
Rendimiento 43.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_03
Fc1ccc(OCCCN2CCC(N3CCc4ccc(Br)cc43)CC2)cc1
Reaction #1877660
title compound
Rendimiento 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_07
OC(c1ccccc1)(c1ccccc1)C12CC[N+](CCCOc3ccc(F)cc3)(CC1)CC2.[Br-]
Reaction #1962828
desired product
Rendimiento 43.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_11
OC(c1ccccc1)(c1ccccc1)C12CC[N+](CCCOc3ccc(F)cc3)(CC1)CC2.[Br-]
Reaction #2014276
desired product
Rendimiento 43.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_05
Fc1ccc(OCCCN2CCC(Oc3ccccc3)CC2)cc1
Reaction #2042359
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_09
OC(c1ccccc1)(c1ccccc1)C12CC[N+](CCCOc3ccc(F)cc3)(CC1)CC2.[Br-]
Reaction #2125481
desired product
Rendimiento 43.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_11
OC(c1ccccc1)(c1ccccc1)C12CC[N+](CCCOc3ccc(F)cc3)(CC1)CC2.[Br-]
Reaction #2254773
desired product
Rendimiento 43.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_06
OCCc1cccc(OCCCOc2ccc(F)cc2)c1
Reaction #2336225
title compound
Rendimiento 95.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1991_08
OC(c1ccccc1)(c1ccccc1)C12CC[N+](CCCOc3ccc(F)cc3)(CC1)CC2.[Br-]
Reaction #2370279
desired product
Rendimiento 43.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_09
Fc1ccc(OCCCN2CCC(N3CCc4ccc(Br)cc43)CC2)cc1
Reaction #2436769
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (10/10)