4-chloropyridine hydrochloride

CC(N)COc1ccncc1
Reaction #1023
desired product
Ausbeute 30.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1ccc(N2CCN(c3ccncc3)CC2)cc1
Reaction #2303
4-[4-(4-pyridyl)-piperazin-1-yl]anisole
Ausbeute 31.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(=O)NC1CCN(c2ccncc2)CC1
Reaction #2326
4-acetylamino-1-(4-pyridyl)piperidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1ccc(Nc2ccncc2)cc1
Reaction #2333
4-(4-pyridylamino)-methoxybenzene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cl.O=C(O)COc1ccc(C(=O)CN2CCN(c3ccncc3)CC2=O)cc1
Reaction #2338
title compound
Ausbeute 40.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cn1ccc2cc(Nc3ccncc3)ccc21
Reaction #5987
solid
Ausbeute 53.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
O=C(O)C1CCN(c2ccncc2)CC1
Reaction #44977
title compound
Ausbeute 78.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cn1ccc2cc(Nc3ccncc3)ccc21
Reaction #49836
solid
Ausbeute 53.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_06
c1ccc(Oc2ccncc2)cc1
Reaction #51445
4-phenoxypyridine
Ausbeute 64.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
O=C(N[C@@H](COCC1CCN(c2ccncc2)CC1)c1ccccc1)c1ccc2c(Cl)c[nH]c2c1
Reaction #60699
3-Chloro-N-[(R)-1-phenyl-2-[1-(4-pyridinyl)piperidin-4-yl-methoxy]ethyl]-1H-indole-6-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CCCN(c1ccncc1)c1c(OC)nn2c(-c3c(OC)cc(COC)cc3OC)csc12
Reaction #69558
title compound
Ausbeute 58.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CCOC(=O)C1CCCN(c2ccncc2)C1
Reaction #78219
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
CCCN(c1ccncc1)N1C(=O)C(C)(C)c2ccccc21
Reaction #82222
desired product
Ausbeute 33.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
O=C(O)c1ccccc1Nc1ccncc1
Reaction #93160
2-(4-pyridinylamino)benzoic acid
Ausbeute 99.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1986_09
O=C(c1ccccc1Nc1ccncc1)N1CCCCC1
Reaction #93163
1-[2-(4-pyridinylamino)benzoyl]piperidine
Ausbeute 65.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1986_09
O=C(O)c1cc(Cl)ccc1Nc1ccncc1
Reaction #93164
5-chloro-2-(4-pyridinylamino)benzoic acid
Ausbeute 40.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1986_09
COc1ccc(Nc2ccncc2)c(C(=O)O)c1
Reaction #93165
5-methoxy-2-(4-pyridinylamino)benzoic acid
Ausbeute 111.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1986_09
CCCN(c1ccncc1)N1C(=O)C(C)(C)c2ccccc21
Reaction #215861
desired product
Ausbeute 33.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_11
CC(C)(C)Cc1nc2cc(S(=O)(=O)CC3CCN(c4ccncc4)CC3)ccc2n1CC1CC1
Reaction #328825
1-(cyclopropylmethyl)-2-neopentyl-5-((1-(pyridin-4-yl)piperidin-4-yl)methylsulfonyl)-1H-benzo[d]imidazole
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
COc1ccc(N2CCN(c3ccncc3)CC2)cc1
Reaction #353909
4-[4-(4-pyridyl)-piperazin-1-yl]anisole
Ausbeute 31.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_07
Seite 1Weiter