Teilstruktursuche

819058

CCOC(=O)c1cnc2ccc(N3CCN(C)CC3)cc2c1Nc1ccc(F)cc1F
Reaction #658
Ausbeute 0.0%
CC1CCc2cc3[nH]c(=O)cc(C(F)(F)F)c3cc2N1CC1CC1
Reaction #40350
4-Trifluoromethyl-7-methyl-6-cyclopropylmethyl-6,7,8,9-tetrahydropyrido[2,3-g]quinolin-2(1H)-one
DOI: 10.6084/m9.figshare.5104873.v1
CCN1c2cc3c(C(F)(F)F)cc(=O)[nH]c3cc2CCC1C
Reaction #40351
4-Trifluoromethyl-7-methyl-6-ethyl-6,7,8,9-tetrahydropyrido[2,3-g]quinolin-2(1H)-one
DOI: 10.6084/m9.figshare.5104873.v1
CC1CCc2cc3[nH]c(=O)cc(C(F)(F)F)c3cc2N1CC(F)(F)F
Reaction #40352
4-Trifluoromethyl-7-methyl-6-(2,2,2-trifluoroethyl)-6,7,8,9-tetrahydropyrido[2,3-g]quinolin-2(1H)-one
DOI: 10.6084/m9.figshare.5104873.v1
CCCN1CCCc2cc3[nH]c(=O)cc(C(F)(F)F)c3cc21
Reaction #40354
4-Trifluoromethyl-6-propyl-6,7,8,9-tetrahydropyrido[2,3-g]quinolin-2(1H)-one
DOI: 10.6084/m9.figshare.5104873.v1
CCN1CCCc2cc3[nH]c(=O)cc(C(F)(F)F)c3cc21
Reaction #40355
4-Trifluoromethyl-6-ethyl-6,7,8,9-tetrahydropyrido[2,3-g]quinolin-2(1H)-one
DOI: 10.6084/m9.figshare.5104873.v1
O=c1cc(C(F)(F)F)c2cc3c(cc2[nH]1)CCCN3CC1CC1
Reaction #40356
4-Trifluoromethyl-6-cyclopropylmethyl-6,7,8,9-tetrahydropyrido[2,3-g]quinolin-2(1H)-one
DOI: 10.6084/m9.figshare.5104873.v1
Cn1c(=O)c(C(=O)NCC(=O)O)c(O)c2cc(N3CCCCC3)ccc21
Reaction #41920
2-(4-hydroxy-1-methyl-2-oxo-6-(piperidin-1-yl)-1,2-dihydroquinoline-3-carboxamido)acetic acid
Ausbeute 8.1%DOI: 10.6084/m9.figshare.5104873.v1
Cn1c(=O)c(C(=O)NCC(=O)O)c(O)c2cc(N3CCOCC3)ccc21
Reaction #41921
2-(4-hydroxy-1-methyl-6-morpholino-2-oxo-1,2-dihydroquinoline-3-carboxamido)acetic acid
Ausbeute 11.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)Nc1ccc2ncc3c(NC(=O)OCC)cc(-c4ccccc4)c(CCC(=O)O)c3c2c1
Reaction #43887
product 22-2
DOI: 10.6084/m9.figshare.5104873.v1
O=c1cc(-c2cccc(OP(=O)(O)O)c2)[nH]c2ccc(N3CCCC3)cc12
Reaction #66922
147
Ausbeute 69.8%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(Cl)nc2ccc(N3CCN(c4cccnc4)C3=O)cc12
Reaction #167216
product
Ausbeute 35.2%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccncc1N1CCN(c2ccc3nc(Cl)cc(C)c3c2)C1=O
Reaction #167226
product
Ausbeute 46.6%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccncc1N1CCN(c2ccc3[nH]c(=O)cc(C)c3c2)C1=O
Reaction #167227
product
Ausbeute 80.8%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccncc1N1CCN(c2ccc3ncccc3c2)C1=O
Reaction #167259
product
Ausbeute 43.7%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc2nccc(Oc3ccc(NC(=O)NC4CC4)c(F)c3)c2cc1NC(=O)OCc1ccccc1
Reaction #177879
DOI: 10.1039/C8SC04228D
Cc1nc2ccc(N3CCC(N(C)C)C3)cc2c(-c2ccc(F)cc2)c1C(=O)C(F)(F)F
Reaction #190948
DOI: 10.1039/C8SC04228D
N#Cc1cnc2cc3c(cc2c1Nc1ccc(F)c(Cl)c1)N(CCCCCl)CCO3
Reaction #192224
DOI: 10.1039/C8SC04228D
O=c1cc(C(F)(F)F)c2cc3c(cc2[nH]1)CCCN3CC1CC1
Reaction #195149
DOI: 10.1039/C8SC04228D
C=CCN1c2ccc3nc(OC(C)C)cc(C(F)(F)F)c3c2OCC1C(C)C
Reaction #198529
DOI: 10.1039/C8SC04228D
Seite 1Weiter