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COC(=O)c1ccc(N)nc1

CCOC(=O)c1ccc(NC(=S)NC(=O)c2ccccc2)nc1
Reaction #6973
ethyl 6-(3-benzoyl-thioureido)-nicotinate
Ausbeute 82.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(NCCCc2ccccc2SCc2ccccc2)nc1
Reaction #11408
named compound
Ausbeute 70.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1ccc(NCCCc2ccccc2SCc2ccccc2)nc1
Reaction #11409
6-[(2-Benzylsulfanylbenzyl)ethylamino]Nicotinic Acid
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc(N2CCC(N)CC2)nc1
Reaction #53513
title product
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1c(C(C)C)nc2c(c1-c1ccc(F)cc1)CCCN2S(C)(=O)=O
Reaction #57368
methyl 4-(4-fluorophenyl)-2-isopropyl-8-methanesulfonyl-5,6,7,8-tetrahydro-[1,8]naphthyridine-3-carboxylate
Ausbeute 86.1%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc(NCCNc2ccc([N+](=O)[O-])cn2)nc1-c1ccccc1
Reaction #60190
final product
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cnc(NCCNc2ccc([N+](=O)[O-])cn2)cc1-c1ccccc1
Reaction #60217
ethyl 6-({2-[(5-nitro(2-pyridyl))amino]ethyl}amino)-4-phenylpyridine-3-carboxylate
Ausbeute 70.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc(N2CCN(c3nnc(Cc4ccccc4)c4ccccc34)C[C@H]2C)nc1
Reaction #70466
title compound
Ausbeute 71.1%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc(N2CCN(c3nnc(Cl)c4ccccc34)CC2)nc1
Reaction #70482
title compound
Ausbeute 49.0%DOI: 10.6084/m9.figshare.5104873.v1
CNc1ncc(C(=O)OC)cc1N
Reaction #78468
Methyl 5-amino-6-methylaminonicotinate
DOI: 10.6084/m9.figshare.5104873.v1
CNc1ncc(C(=O)OC)cc1NC(=O)CCc1ccc(C#N)cc1
Reaction #78469
crude product
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cnc([N+](=O)[O-])c(OCc2ccccc2F)c1
Reaction #92685
methyl 5-[(2-fluorobenzyl)oxy]-6-nitronicotinate
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cnc(N)c(OCc2ccccc2F)c1
Reaction #92686
methyl 6-amino-5-[(2-fluorobenzyl)oxy]nicotinate
Ausbeute 99.8%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(OCc2ccccc2F)c2nc(C)cn2c1
Reaction #92687
methyl 8-[(2-fluorobenzyl)oxy]-2-methylimidazo[1,2-a]pyridine-6-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cnc(N2CCC[C@H]2C(=O)OC)c([N+](=O)[O-])c1
Reaction #156760
title compound
Ausbeute 94.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cnc2c(c1)NC(=O)[C@@H]1CCCN21
Reaction #156761
title compound
Ausbeute 80.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc(N2CCN(Cc3cnc4c(c3)NC(=O)[C@@H]3CCCN43)CC2)nc1
Reaction #156764
title compounds
Ausbeute 77.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc(N2CCN(Cc3cnc4c(c3)NC(=O)[C@@H]3CCCCN43)CC2)nc1
Reaction #156817
title compound
Ausbeute 89.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cnc2c(c1)NC(=O)CN2Cc1ccccc1
Reaction #156830
title compound
Ausbeute 71.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1CN(Cc2ccccc2)c2ncc(CO)cc2N1
Reaction #156831
title compound
Ausbeute 99.3%DOI: 10.6084/m9.figshare.5104873.v1
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