An 12 Reaktionen beteiligt

CCO.CNC

COc1ccnc(Br)c1
Reaction #53240
4-methoxy-2-bromopyridine
Ausbeute 22.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
—
Reaction #1127580
oil
Ausbeute 19.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_10
CN(C)c1ccnc(Cl)n1
Reaction #1369350
title compound
Ausbeute 59.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_09
CC(=O)N1CCN(c2nc(F)cc(N(C)C)n2)CC1
Reaction #1369362
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_09
CC(=O)N1CCN(c2nc(N(C)C)cc(N(C)C)n2)CC1
Reaction #1369363
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_09
CC(=O)N1CCc2c(sc(C)c2CCN(C)C)C1
Reaction #1821236
6-acetyl-3-(2-dimethylaminoethyl)-4,5,6,7-tetrahydro-2-methylthieno[2,3-c]pyridine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_07
CN(C)C(=O)c1ccccc1C=O
Reaction #1941874
title compound
Ausbeute 19.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_02
CN(C)c1ccccc1C=O
Reaction #1941882
title compound
Ausbeute 85.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_02
CN(C)c1cc(Br)ccc1C=O
Reaction #1941900
title compound
Ausbeute 81.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_02
CN(C)c1cc(N2CCN(C(=O)c3ccccc3)CC2)ccc1[N+](=O)[O-]
Reaction #2053623
(4-(3-(dimethylamino)-4-nitrophenyl)piperazin-1-yl)(phenyl)methanone
Ausbeute 21.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_04
CN(C)CC(O)COc1ccc2c(c1)C(=O)CCC2c1ccc(Cl)cc1
Reaction #2146503
4-(4-chlorophenyl)-7-(2-hydroxy-3-dimethylaminopropoxy)-1-tetralone
Ausbeute 71.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_03
CC(=O)N1CCc2c(sc(C)c2CCN(C)C)C1
Reaction #2382009
6-acetyl-3-(2-dimethylaminoethyl)-4,5,6,7-tetrahydro-2-methylthieno[2,3-c]pyridine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_11