Busqueda de Subestructura

14923

CN(c1ccc(F)cc1)c1cc(CO)ccn1
Reaction #354
Rendimiento 0.0%
OCc1ccnc(Cl)c1
Reaction #43335
compound
Rendimiento 908.5%DOI: 10.6084/m9.figshare.5104873.v1
Fc1ccc(OCc2ccnc(Cl)c2)cc1
Reaction #43336
title compound
Rendimiento 51.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)OCC2(O)Cn3c(=O)ccc4ncc(F)c2c43)cc1
Reaction #43398
[(4R/S)-3-Fluoro-4-hydroxy-7-oxo-4,5-dihydro-7H-pyrrolo[3,2,1-de]-1,5-naphthyridin-4-yl]methyl 4-methylbenzenesulfonate
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)OCC2(O)Cn3c(=O)ccc4ncc(Cl)c2c43)cc1
Reaction #43404
product
Rendimiento 95.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NC1CCN(CC2(O)Cn3c(=O)ccc4ncc(Cl)c2c43)CC1
Reaction #43405
product
Rendimiento 85.7%DOI: 10.6084/m9.figshare.5104873.v1
O=c1c(F)cc2ncc(F)c3c2n1CC3(O)CO
Reaction #43415
solid
Rendimiento 97.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)OCC2(O)Cn3c(=O)c(F)cc4ncc(F)c2c43)cc1
Reaction #43416
desired compound
Rendimiento 105.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NC1CCN(CC2(O)Cn3c(=O)c(F)cc4ncc(F)c2c43)CC1
Reaction #43417
1,1-dimethylethyl (1-{[3,8-difluoro-4-hydroxy-7-oxo-4,5-dihydro-7H-pyrrolo[3,2,1-de]-1,5-naphthyridin-4-yl]methyl}-4-piperidinyl)carbamate
DOI: 10.6084/m9.figshare.5104873.v1
NC1CCN(C[C@]2(O)Cn3c(=O)c(F)cc4ncc(F)c2c43)CC1
Reaction #43418
(4S)-4-[(4-amino-1-piperidinyl)methyl]-3,8-difluoro-4-hydroxy-4,5-dihydro-7H-pyrrolo[3,2,1-de]-1,5-naphthyridin-7-one
DOI: 10.6084/m9.figshare.5104873.v1
Cl.Cl.O=c1c(F)cc2ncc(F)c3c2n1C[C@@]3(O)CN1CCC(NCc2cc3c(cn2)OCS3)CC1
Reaction #43419
title compound
Rendimiento 36.0%DOI: 10.6084/m9.figshare.5104873.v1
O=c1c(F)cc2ncc(F)c3c2n1CC3(O)CO
Reaction #43434
solid
Rendimiento 82.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NC1CCN(CC2(O)Cn3c(=O)c(Cl)cc4ncc(F)c2c43)CC1
Reaction #43440
1,1-dimethylethyl {1-[((4R/S)-8-chloro-3-fluoro-4-hydroxy-7-oxo-4,5-dihydro-7H-pyrrolo[3,2,1-de]-1,5-naphthyridin-4-yl)methyl]-4-piperidinyl}carbamate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NC1CCN(CC2(F)Cn3c(=O)ccc4ncc(F)c2c43)CC1
Reaction #43442
product
Rendimiento 33.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)N
Reaction #43444
isopropylamine
DOI: 10.6084/m9.figshare.5104873.v1
Br.Cc1ncc(CBr)c(CO)c1O
Reaction #47748
3-Bromomethyl-5-hydroxy-4-hydroxymethyl-6-methylpyridine hydrobromide
DOI: 10.6084/m9.figshare.5104873.v1
Clc1ccc2c(c1)CCc1cccnc1C2N1CCN(Cc2ccncc2)CC1
Reaction #49693
(+)-8-chloro-6,11-dihydro-11-[4-(4-pyridinylmethyl)-1-piperazinyl]-5h-benzo[5,6]cyclohepta-[1,2-b]pyridine
Rendimiento 75.5%DOI: 10.6084/m9.figshare.5104873.v1
Clc1ccc2c(c1)CCc1cccnc1C2N1CCN(Cc2ccncc2)CC1
Reaction #49694
(-)-8-chloro-6,11-dihydro-11-[4 -(4-pyridinylmethyl)-1-piperazinyl]-5h-benzo[5,6]cyclohepta-[1,2-b]pyridine
Rendimiento 45.3%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(CN(C)CC(O)c2ccncc2)sc2c(=O)c(C(=O)NCc3ccc(Cl)cc3)cn(C)c12
Reaction #51946
title compound
Rendimiento 65.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cncc(O)c1C(=O)OC
Reaction #65741
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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