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1352462

CCNC(=O)Nc1nc2nc(NCCCCN(CC)CC)ncc2cc1-c1c(Cl)cccc1Cl.Cl
Reaction #3536
hydrochloric acid
DOI: 10.6084/m9.figshare.5104873.v1
N=C(N)c1ccccc1-c1ccc(C(=O)Nc2ccccc2C(=O)Nc2ccc(Cl)cn2)cc1
Reaction #40410
2-[4-(N-{2-[N-(5-chloro-2-pyridyl)carbamoyl]phenyl}carbamoyl)phenyl]benzenecarboxamidine
収率 15.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1ccccc1C(=O)Nc1ccc(Cl)cn1)c1ccc(-c2ccccc2C=NNO)cc1
Reaction #40411
N-{2-[N-(5-chloro(2-pyridyl))carbamoyl]phenyl}{4-[2-((hydroxyamino)iminomethyl)phenyl]phenyl}carboxamide
収率 27.5%DOI: 10.6084/m9.figshare.5104873.v1
NCc1ccccc1-c1ccc(C(=O)Nc2ccccc2C(=O)Nc2ccc(Cl)cn2)cc1
Reaction #40412
{4-[2-(aminomethyl)phenyl]phenyl)-N-(2-[N-(5-chloro(2-pyridyl))carbamoyl]phenyl}carboxamide
収率 43.1%DOI: 10.6084/m9.figshare.5104873.v1
N=C(N)c1ccccc1-c1ccc(C(=O)Nc2ccccc2C(=O)Nc2ccc(Cl)cn2)cc1
Reaction #40439
2-[4-(N-{2-[N-(5-chloro-2-pyridyl)carbamoyl]phenyl}carbamoyl)phenyl]benzenecarboxamidine
収率 15.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1ccccc1C(=O)Nc1ccc(Cl)cn1)c1ccc(-c2ccccc2C=NNO)cc1
Reaction #40440
N-{2-[N-(5-chloro(2-pyridyl))carbamoyl]phenyl}{4-[2-((hydroxyamino)iminomethyl)phenyl]phenyl}carboxamide
収率 27.5%DOI: 10.6084/m9.figshare.5104873.v1
NCc1ccccc1-c1ccc(C(=O)Nc2ccccc2C(=O)Nc2ccc(Cl)cn2)cc1
Reaction #40441
{4-[2-(aminomethyl)phenyl]phenyl}-N-{2-[N-(5-chloro(2-pyridyl))carbamoyl]phenyl}carboxamide
収率 43.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CN(C(=O)CCl)c1nc(-c2ccccc2Cl)c(-c2ccc(Cl)cc2)cc1C#N
Reaction #42114
2-chloro-N-(6-(2-chlorophenyl)-5-(4-chlorophenyl)-3-cyanopyridin-2-yl)-N-isobutylacetamide
DOI: 10.6084/m9.figshare.5104873.v1
COCCN1Cc2cc(/C=C/C(=O)N(C)Cc3c(C)[nH]c4ccccc34)cnc2NC1=O
Reaction #46626
title compound
収率 36.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1c(C(C)C)nc2c(c1-c1ccc(F)cc1)CCCN2
Reaction #57367
methyl 4-(4-fluorophenyl)-2-isopropyl-5,6,7,8-tetrahydro-[1,8]naphthyridine-3-carboxylate
収率 92.1%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CCN(C)CC(=O)N2c3ccccc3C(=O)Nc3cccnc32)cc1
Reaction #65133
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CCN(C(=O)c1cnc2c(c1)nc(CCc1ccc(C(=N)N)cc1)n2C)c1ccccn1.Cl
Reaction #78472
3-Methyl-2-[2-(4-amidinophenyl)ethyl]imidazo[4,5-b]pyridin-6-yl-carboxylic acid-N-(2-pyridyl)-N-(2-methoxycarbonylethyl)amide hydrochloride
収率 75.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCNC(=O)OC1c2ccccc2C(=O)N1c1ccc2ccc(Cl)nc2n1
Reaction #94610
2-(7-chloro-1,8-naphthyridin-2-yl)-3-propylaminocarbonyloxy-isoindolin-1-one
収率 178.4%DOI: 10.6084/m9.figshare.5104873.v1
CCC(C)NC(=O)OC1c2ccccc2C(=O)N1c1ccc2ccc(Cl)nc2n1
Reaction #94611
2-(7-Chloro-1,8-naphthyridin-2-yl)-3-sec-butylaminocarbonyloxy-isoindolin-1-one
DOI: 10.6084/m9.figshare.5104873.v1
O=C(NC1CC1)OC1c2ccccc2C(=O)N1c1ccc2ccc(Cl)nc2n1
Reaction #94612
2-(7-chloro-1,8-naphthyridin-2-yl)-3-cyclopropylaminocarbonyloxy-isoindolin-1-one
収率 81.4%DOI: 10.6084/m9.figshare.5104873.v1
CCCCNC(=O)OC1c2ccccc2C(=O)N1c1ccc2ccc(Cl)nc2n1
Reaction #94618
2-(7-chloro-1,8 naphtyridin-2-yl)-3-n-butylaminocarbonyloxy-isoindolin-1-one
収率 46.7%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CNC(=O)OC1c2ccccc2C(=O)N1c1ccc2ccc(Cl)nc2n1
Reaction #94619
2-(7-chloro-1,8-naphthyridin-2-yl)-3-methoxycarbonylmethylaminocarbonyloxy-isoindolin-1-one
収率 57.1%DOI: 10.6084/m9.figshare.5104873.v1
CCCCNC(=O)OC1c2cc(Cl)ccc2C(=O)N1c1ccc2ccc(Cl)nc2n1
Reaction #94623
5-chloro-2-(7-chloro-1,8-naphthyridin-2-yl)-3-n-butylaminocarbonyloxy-isoindolin-1-one
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)Nc1ccc(C(=O)NC2=Nc3cc(N4CCOCC4)ccc3C3=NCCN23)cn1
Reaction #174402
DOI: 10.1039/C8SC04228D
CNCc1csc(C(=O)Nc2ccc(Cl)cc2C(=O)Nc2ccc(Cl)cn2)c1Cl
Reaction #177743
DOI: 10.1039/C8SC04228D
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