부분 구조 검색

670

c1ccc(CNc2ccnc(Nc3ccccc3)c2)cc1
Reaction #634
수율 6.3%
c1ccc(CNc2ccnc(Nc3ccccc3)c2)cc1
Reaction #637
수율 36.9%
c1ccc(CNc2ccnc(Nc3ccccc3)c2)cc1
Reaction #638
수율 42.0%
c1ccc(Nc2ncco2)nc1
Reaction #674
수율 0.0%
CNc1cc(Nc2ccccc2[N+](=O)[O-])ncn1
Reaction #86405
title compound
수율 35.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)c(Cl)c(N(COCC[Si](C)(C)C)C(=O)N(C)c2cc(Nc3ccc(N4CCN(C(=O)OC(C)(C)C)CC4)cc3[N+](=O)[O-])ncn2)c1Cl
Reaction #86480
title compound
수율 45.3%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H]1CC[C@H](Cn2c(Nc3ccccc3)nc3cc(C#N)nc(-c4cncc(Cl)c4)c32)CC1
Reaction #168379
4-(5-chloropyridin-3-yl)-3-[(trans-4-methylcyclohexyl)methyl]-2-(phenylamino)-3H-imidazo[4,5-c]pyridine-6-carbonitrile
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2cc(-c3ccc(F)cc3C)sc2c1
Reaction #420031
2-(4-fluoro-2-methylphenyl)-6-methoxybenzo[b]thiophene
수율 44.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(F)cncc1-c1cc2cnc(NC(=O)OC(C)(C)C)cc2c[n+]1[O-]
Reaction #556137
title compound
수율 38.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(F)cncc1-c1cc2cnc(NC(=O)C3CC3)cc2c[n+]1[O-]
Reaction #556143
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ncccc1-c1nccnc1Oc1ccc(Nc2ccccn2)cc1
Reaction #560818
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(Nc2ccc(Oc3ncccc3C3CCOCC3)cc2)nc1
Reaction #560824
5-methyl-N-(4-(3-(tetrahydro-2H-pyran-4-yl)pyridin-2-yloxy)phenyl)pyridin-2-amine
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(Nc2ccc(Oc3nccnc3C3CCOCC3)cc2)nc1
Reaction #560861
5-methyl-N-(4-(3-(tetrahydro-2H-pyran-4-yl)pyrazin-2-yloxy)phenyl)pyridin-2-amine
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)[C@@H](OC(C)(C)C)c1c(C)cc2cc(C(=O)NC)c(F)cc2c1OS(=O)(=O)C(F)(F)F
Reaction #601289
solid
수율 13.9%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cnc(Nc2ccc(C(=O)O)cc2[N+](=O)[O-])nc1N1CCN(C(=O)OC(C)(C)C)CC1
Reaction #611269
title compound
수율 34.1%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(S(=O)(=O)C2CCN(c3c(N)cncc3F)CC2)CC1
Reaction #612088
5-fluoro-4-(4-((4-methylpiperazin-1-yl)sulfonyl)piperidin-1-yl)pyridin-3-amine
DOI: 10.6084/m9.figshare.5104873.v1
CN1CC=C(c2c(F)cncc2NC(=O)OC(C)(C)C)CC1
Reaction #612134
tert-butyl (5-fluoro-1′-methyl-1′,2′,3′,6′-tetrahydro-[4,4′-bipyridin]-3-yl)carbamate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)Nc1cncc(F)c1C1=CCN(C2COC2)CC1
Reaction #612140
tert-butyl (5-fluoro-1′-(oxetan-3-yl)-1′,2′,3′,6′-tetrahydro-[4,4′-bipyridin]-3-yl)carbamate
수율 24.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)Nc1nccc2ccc(C(=O)O)cc12
Reaction #624383
1-(tert-butylamino)isoquinoline-7-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
COC/C=C/c1nn(C(c2ccccc2)(c2ccccc2)c2ccccc2)c2cc(NC(=O)N[C@H](C)c3ccccc3)ncc12
Reaction #658569
(R,E)-1-(3-(3-methoxyprop-1-en-1-yl)-1-trityl-1H-pyrazolo[4,3-c]pyridin-6-yl)-3-(1-phenylethyl)urea
DOI: 10.6084/m9.figshare.5104873.v1
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