Substructure Search

O=Cc1cccnc1

Cl.N[C@H]1CCN(c2c(F)cc3c(=O)c(C(=O)O)cn(C4CC4)c3c2Cl)C1
Reaction #1406
7-[(S)-3-amino-1-pyrrolidinyl]-8-chloro-1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
NC1CCN(c2c(F)cc3c(=O)c(C(=O)O)cn(C4CC4)c3c2Cl)C1
Reaction #1413
7-(3-amino-1-pyrrolidinyl)-8-chloro-1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1ccc(=O)[nH]c1Nc1ccc(Br)cc1F
Reaction #44222
pure desired product
Yield 83.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1ccc(=O)[nH]c1Nc1ccc(Br)cc1F
Reaction #44223
pure desired product
Yield 93.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1c(C(C)C)nc(N)c(/C=C/CCOCc2ccccc2)c1-c1ccc(F)cc1
Reaction #57363
methyl (E)-6-amino-5-(4-(phenylmethoxy)but-1-enyl)-4-(4-fluorophenyl)-2-(1-methylethyl)nicotinate
Yield 82.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cnc(NCCNc2ccc(C(=O)N3CCOCC3)cn2)nc1-c1ccc(C#N)cc1
Reaction #60033
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc(C#C/C=C/C23OC2(C)CCCC3(C)C)nc1
Reaction #81518
Ethyl (±)-6-[(3E)-4-(1,2-Epoxy-2,6,6-trimethylcyclohexanyl)but-3-en-1-ynyl)nicotinate
DOI: 10.6084/m9.figshare.5104873.v1
CCNc1ncccc1C(=O)Nc1c(C)ccnc1Cl
Reaction #81798
title compound
Yield 76.2%DOI: 10.6084/m9.figshare.5104873.v1
Cl
Reaction #172981
DOI: 10.1039/C8SC04228D
CC1CN(c2c(F)cc3c(=O)c(C(=O)O)cn(C4CC4)c3c2F)CC1NC(=O)OC(C)(C)C
Reaction #176325
DOI: 10.1039/C8SC04228D
O=C(O)c1cccnc1Nc1cc(Cl)cc(Cl)c1
Reaction #178675
DOI: 10.1039/C8SC04228D
C=C1CCCN(C(=O)c2ccc(NC(=O)c3ccccc3C)nc2)c2ccc(Cl)cc21
Reaction #181785
DOI: 10.1039/C8SC04228D
CCn1c(-c2nonc2N)nc2cnc(Oc3cccc(NC(=O)c4ccc(=O)[nH]c4)c3)cc21
Reaction #182771
DOI: 10.1039/C8SC04228D
CC(C)CCNC(=O)c1ccc(N2CCN(C(=O)c3cnccc3C(F)(F)F)CC2)nn1
Reaction #184129
DOI: 10.1039/C8SC04228D
Cc1nnc(-c2cccc(OCc3csc4c(C(=O)NCCO)cnc(N)c34)c2)o1
Reaction #198485
DOI: 10.1039/C8SC04228D
CC(C(=O)O)c1ccc(N2CCN(c3ccc(C(=O)Nc4cccc(C(C)(C)C)c4)cn3)CC2)cc1
Reaction #199096
DOI: 10.1039/C8SC04228D
CN1CCN(c2ccc(Nc3nc(-c4ccncc4)c(F)cc3C(N)=O)cc2)CC1
Reaction #202531
DOI: 10.1039/C8SC04228D
COC(=O)c1c(C(C)C)nc(N)c(C=CCCOCc2ccccc2)c1-c1ccc(F)cc1
Reaction #205965
DOI: 10.1039/C8SC04228D
CCSc1nc2cc(C(F)(F)F)ccc2c(N(C)C)c1C(=O)NCc1cccc(F)c1
Reaction #210089
DOI: 10.1039/C8SC04228D
Cc1ccccc1CC(=O)Nc1ccc(C(=O)N2Cc3cccn3Cc3ccccc32)cn1
Reaction #223405
DOI: 10.1039/C8SC04228D
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