Busqueda de Subestructura

830670

COc1ccc(F)c(-c2ccc3nc(N[C@@H]4CCC[C@@H]4NC(=O)OC(C)(C)C)ncc3c2)c1F
Reaction #84634
tert-butyl ((1S,2R)-2-((6-(2,6-difluoro-3-methoxyphenyl)quinazolin-2-yl)amino)cyclopentyl)carbamate
Rendimiento 74.4%DOI: 10.6084/m9.figshare.5104873.v1
CCOc1ccc(F)c(-c2ccc3nc(N[C@@H]4CCC[C@@H]4NC(=O)OC(C)(C)C)ncc3c2)c1Cl
Reaction #84638
tert-butyl ((1S,2R)-2-((6-(2-chloro-3-ethoxy-6-fluorophenyl)quinazolin-2-yl)amino)cyclopentyl)carbamate
Rendimiento 84.8%DOI: 10.6084/m9.figshare.5104873.v1
COc1c(-c2ccc3nc(N[C@@H]4CCC[C@@H]4NC(=O)OC(C)(C)C)ncc3c2)ccc(C(=O)O)c1C
Reaction #84642
methyl 4-(2-(((1R,2S)-2-((tert-butoxycarbonyl)amino)cyclopentyl)amino)quinazolin-6-yl)-3-methoxybenzoic acid
Rendimiento 96.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(-c2c(C(C)N=[N+]=[N-])nc3scc(C)n3c2=O)cc1
Reaction #86562
desired product
Rendimiento 61.5%DOI: 10.6084/m9.figshare.5104873.v1
Cc1csc2nc(C(C)N=[N+]=[N-])c(-c3ccccc3F)c(=O)n12
Reaction #86566
desired product
Rendimiento 69.5%DOI: 10.6084/m9.figshare.5104873.v1
Cc1csc2nc(C(C)N=[N+]=[N-])c(-c3cccc(F)c3F)c(=O)n12
Reaction #86568
desired product
Rendimiento 62.9%DOI: 10.6084/m9.figshare.5104873.v1
Cc1csc2nc(C(C)N=[N+]=[N-])c(-c3cncc(F)c3)c(=O)n12
Reaction #86572
desired product
Rendimiento 16.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1csc2nc(C(C)N=[N+]=[N-])c(-c3ccccc3Cl)c(=O)n12
Reaction #86574
desired product
Rendimiento 47.2%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #86577
mixture
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(C2CC2)cc1O
Reaction #167943
4-cyclopropyl-2-hydroxybenzonitrile
DOI: 10.6084/m9.figshare.5104873.v1
CC1Cc2ccc(-c3ccn(CC#N)n3)cc2CN1c1cc(N2CCN(C)CC2)nc(N)n1
Reaction #286951
DOI: 10.1039/C8SC04228D
C=Cc1cnc(F)c(-c2nc(C)nc3c2ncn3C2CCCCO2)c1
Reaction #374273
DOI: 10.1039/C8SC04228D
COc1cn(Cc2ccccc2)nc(-c2ccnn2-c2ccccc2)c1=O
Reaction #420907
title compound
Rendimiento 77.7%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)OCCc2c1sc1c(N3CCOCC3)nc(-c3cnc(N)nc3)nc21
Reaction #421338
168
Rendimiento 22.6%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)OCCn2c1cc1c(N3CCOCC3)nc(-c3cnc(N)nc3)nc12
Reaction #421361
177
Rendimiento 15.0%DOI: 10.6084/m9.figshare.5104873.v1
NC1=N[C@@]2(CO1)c1cc(Br)ccc1Oc1ccc(-c3ccccc3)cc12
Reaction #422952
(R)-2′-bromo-7′-phenyl-5H-spiro[oxazole-4,9′-xanthen]-2-amine
DOI: 10.6084/m9.figshare.5104873.v1
NC1=NC2(CO1)c1cc(-c3cccnc3)ccc1Oc1c2cc(-c2cccnc2)nc1F
Reaction #422979
1-fluoro-3,7-di(pyridin-3-yl)-5′H-spiro[chromeno[2,3-c]pyridine-5,4′-oxazol]-2′-amine
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cnc(F)c(-c2ccc3c(c2)[C@@]2(COC(N)=N2)c2cc(C4=CCOCC4)ncc2O3)c1
Reaction #422985
(S)-3-(3,6-dihydro-2H-pyran-4-yl)-7-(2-fluoro-5-methylpyridin-3-yl)-5′H-spiro[chromeno[2,3-c]pyridine-5,4′-oxazol]-2′-amine
DOI: 10.6084/m9.figshare.5104873.v1
NC1=N[C@@]2(CO1)c1cc(-c3cccnc3F)ccc1Oc1cnc(C3=CCOCC3)cc12
Reaction #422990
(S)-3-(3,6-dihydro-2H-pyran-4-yl)-7-(2-fluoropyridin-3-yl)-5′H-spiro[chromeno[2,3-c]pyridine-5,4′-oxazol]-2′-amine
DOI: 10.6084/m9.figshare.5104873.v1
NC1=N[C@@]2(CO1)c1cc(-c3c(F)ccnc3F)ccc1Oc1cnc(C3=CCOCC3)cc12
Reaction #423000
desired product
DOI: 10.6084/m9.figshare.5104873.v1
Página 1Siguiente