#5944546

N#CCc1cc(F)cc(Br)c1
Reaction #79020
3-Bromo-5-fluorophenylacetonitrile
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
CC(C)(C)OC(=O)CN(Cc1cc(F)cc(Br)c1)S(=O)(=O)c1ccc2c(c1)CCC(C)(C)O2
Reaction #245791
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(C)(C)OC(=O)N1CCC(COCc2cc(F)cc(Br)c2)(c2ccccc2)CC1
Reaction #478609
tert-Butyl 4-((3-bromo-5-fluorobenzyloxy)methyl)-4-phenylpiperidine-1-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_02
N#CCc1cc(F)cc(Br)c1
Reaction #500367
3-Bromo-5-fluorophenylacetonitrile
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_05
O=c1n(Cc2cc(F)cc(Br)c2)nc(-c2ccc(Cl)cc2)n1C[C@H](O)C(F)(F)F
Reaction #801841
2-(3-Bromo-5-fluorobenzyl)-5-(4-chlorophenyl)-4-[(2S)-3,3,3-trifluoro-2-hydroxypropyl]-2,4-dihydro-3H-1,2,4-triazol-3-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_11
N#CCc1cc(F)cc(Br)c1
Reaction #886028
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CCC(COCc2cc(F)cc(Br)c2)(c2ccccc2)CC1
Reaction #1210788
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (7/10)
N#CCc1cc(F)cc(Br)c1
Reaction #1365873
3-Bromo-5-fluorophenylacetonitrile
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_09
COC1=N[C@H](C(C)C)C(OC)=N[C@H]1Cc1cc(F)cc(Br)c1
Reaction #1558828
(2S,5R)-2-(3-bromo-5-fluorobenzyl)-5-isopropyl-3,6-dimethoxy-2,5-dihydropyrazine
Выход 85.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_04
N#CCc1cc(F)cc(Br)c1
Reaction #1722177
3-Bromo-5-fluorophenylacetonitrile
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_01
N#CCc1cc(F)cc(Br)c1
Reaction #1812259
3-Bromo-5-fluorophenylacetonitrile
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_02
CC(C)(C)OC(=O)CN(Cc1cc(F)cc(Br)c1)S(=O)(=O)c1ccc2c(c1)CCC(C)(C)O2
Reaction #1893136
powder
Выход 90.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_01
N#CCc1cc(F)cc(Br)c1
Reaction #1970034
3-Bromo-5-fluorophenylacetonitrile
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_07