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162575

CC1CN(c2c(F)cc3c(=O)c(C(=O)O)cn(C4CC4)c3c2Cl)CC1N
Reaction #196765
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)NC12CCC1CN(c1c(F)cc3c(=O)c(C(=O)O)cn(C4CC4)c3c1Cl)C2
Reaction #211450
DOI: 10.1039/C8SC04228D
O=C(Cc1ccccc1)N[C@@H]1C(=O)N2C(C(=O)OC(c3ccccc3)c3ccccc3)=C(CN3CCC[C@H]4CN(c5c(F)cc6c(=O)c(C(=O)O)cn(C7CC7)c6c5Cl)C[C@H]43)CS[C@H]12
Reaction #461737
title product
DOI: 10.6084/m9.figshare.5104873.v1
CC1CN(c2c(F)cc3c(=O)c(C(=O)O)cn(C4CC4)c3c2Cl)CC1NC(=O)OC(C)(C)C
Reaction #667754
title compound
Выход 50.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1CN(c2c(F)cc3c(=O)c(C(=O)O)cn(C4CC4)c3c2Cl)CC1N
Reaction #667755
title compound
Выход 25.3%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H]1CN(c2c(F)cc3c(=O)c(C(=O)O)cn(C4CC4)c3c2Cl)C[C@H]1N
Reaction #667764
title compound
Выход 73.2%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CN(c2c(F)cc3c(=O)c(C(=O)O)cn(C4CC4)c3c2Cl)C[C@H]1NC(=O)OC(C)(C)C
Reaction #667765
7-(trans-3-t-butoxycarbonylamino-4-methyl-1-pyrrolidinyl)-8-chloro-1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid
Выход 102.7%DOI: 10.6084/m9.figshare.5104873.v1
CC1CN(c2c(F)cc3c(=O)c(C(=O)O)cn(C4CC4)c3c2Cl)CC1NC(=O)OC(C)(C)C
Reaction #888472
DOI: 10.1039/C8SC04228D
O=C(Cc1ccccc1)NC1C(=O)N2C(C(=O)OC(c3ccccc3)c3ccccc3)=C(CN3CCCC4CN(c5c(F)cc6c(=O)c(C(=O)O)cn(C7CC7)c6c5Cl)CC43)CSC12
Reaction #892832
DOI: 10.1039/C8SC04228D
CN1CCC2CN(c3c(F)cc4c(=O)c(C(=O)O)cn(C5CC5)c4c3Cl)CC21
Reaction #1214510
DOI: 10.1039/C8SC04228D
NC1CN(c2c(F)cc3c(=O)c(C(=O)O)cn(C4CC4)c3c2Cl)CC12CC2
Reaction #1316540
DOI: 10.1039/C8SC04228D
CN1CCC2CN(c3c(F)cc4c(=O)c(C(=O)O)cn(C5CC5)c4c3Cl)CC21
Reaction #1547927
8-chloro-1-cyclopropyl-6-fluoro-1,4-dihydro-7-(2-methyl-2,7-diazabicyclo[3.3.0]oct-7-yl)-4-oxo-3-quinolinecarboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
Cl.N[C@@]12C=CC=C[C@@H]1CN(c1c(F)cc3c(=O)c(C(=O)O)cn([C@@H]4C[C@@H]4F)c3c1Cl)C2
Reaction #1576733
7-[(3aS,7aR)3a-amino-1,2,3,7a-tetrahydro-isoindol-2-yl]-8-chloro-1-[(1R,2S)-2-fluorocyclopropyl]-6-fluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NC12CCC1CN(c1c(F)cc3c(=O)c(C(=O)O)cn(C4CC4)c3c1Cl)C2
Reaction #1690620
7-[1-(t-butoxycarbonylamino)-3-azabicyclo[3.2.0]hept-3-yl]-8-chloro-1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxoquinoline-3-carboxylic acid
Выход 60.9%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCC2CN(c3c(F)cc4c(=O)c(C(=O)O)cn(C5CC5)c4c3Cl)CC21
Reaction #1733154
8-chloro-1-cyclopropyl-6-fluoro-1,4-dihydro-7-(2-methyl-2,7-diazabicyclo[3.3.0]oct-7-yl)-4-oxo-3-quinolinecarboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
NC1CN(c2c(F)cc3c(=O)c(C(=O)O)cn(C4CC4)c3c2Cl)CC12CC2
Reaction #1808271
7-(7-amino-5-azaspiro[2.4]heptane-5-yl)-8-chloro-1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxoquinoline-3-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NC1CN(c2c(F)cc3c(=O)c(C(=O)O)cn(C4CC4)c3c2Cl)CC12CC2
Reaction #1808277
7-(7-tert-butoxycarbonylamino-5-azaspiro[2.4]heptan-5-yl)-8-chloro-1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxoquinoline-3-carboxylic acid
Выход 74.6%DOI: 10.6084/m9.figshare.5104873.v1
NC1CN(c2c(F)cc3c(=O)c(C(=O)O)cn(C4CC4)c3c2Cl)CC12CC2
Reaction #2062508
7-(7-amino-5-azaspiro[2,4]heptane-5-yl)-8-chloro-1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxoquinoline-3-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NC1CN(c2c(F)cc3c(=O)c(C(=O)O)cn(C4CC4)c3c2Cl)CC12CC2
Reaction #2062515
7-(7-tert-butoxycarbonylamino-5-azaspiro[2,4]heptan-5-yl)-8-chloro-1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxoquinoline-3-carboxylic acid
Выход 74.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC[C@H]2CN(c3c(F)cc4c(=O)c(C(=O)O)cn([C@@H]5C[C@@H]5F)c4c3Cl)C[C@H]21
Reaction #2343266
titled compound
Выход 55.9%DOI: 10.6084/m9.figshare.5104873.v1
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