An 46 Reaktionen beteiligt

920

COc1cc(NC2COC2)ccc1Br
Reaction #728
Ausbeute 35.8%750 AstraZeneca ELN dataset
FC(F)(F)COCc1cc(NC2COC2)nc(Cl)n1
Reaction #87384
title compound
Ausbeute 55.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CC1(C)c2cc(C(=O)NC3COC3)ccc2C(=O)c2c1[nH]c1cc(C#N)ccc21
Reaction #90046
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
Nc1ccc(-c2cccs2)cc1NC(=O)NC1COC1
Reaction #90968
1-(2-amino-5-(thiophen-2-yl)phenyl)-3-(oxetan-3-yl)urea
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
Clc1ncnc2c1ccn2C1COC1
Reaction #169360
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC(CC1CN(S(=O)(=O)c2cccs2)CCN1c1ccc(C(C)(O)C(F)(F)F)cc1)NC1COC1
Reaction #185857
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(N1CCOCC1)N1CC(c2ccc(C(F)(F)F)cc2)CC(c2nc(NC3COC3)no2)C1
Reaction #232485
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cn1ncc(C(=O)NC2COC2)c1C(=O)Nc1ccn2nc(-c3ccccc3)nc2c1
Reaction #278308
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
O=[N+]([O-])c1cc2n(n1)CCN(C1COC1)C2
Reaction #424487
2-nitro-5-oxetan-3-yl-4,5,6,7-tetrahydro-pyrazolo[1,5-a]pyrazine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
Nc1cc(-n2cc(C(=O)O)c(=O)c3cc(F)c(NC4COC4)c(Cl)c32)c(F)cc1F
Reaction #456518
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_10
O=[N+]([O-])c1cc2n(n1)CCN(C1COC1)C2
Reaction #536872
2-nitro-5-oxetan-3-yl-4,5,6,7-tetrahydro-pyrazolo[1,5-a]pyrazine
Ausbeute 71.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_07
CSc1nc(C(F)(F)c2ccc(F)cn2)nc2c(C(=O)NC3COC3)cccc12
Reaction #560388
2-(difluoro(5-fluoropyridin-2-yl)methyl)-4-(methylthio)-N-(oxetan-3-yl)quinazoline-8-carboxamide
Ausbeute 266.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_01
O=C(Nc1ccc(C(=O)C2CCN(Cc3ccc(C(O)(C(F)(F)F)C(F)(F)F)cc3)CC2)cc1)NC1COC1
Reaction #602532
title compound
Ausbeute 20.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_08
N#Cc1ccc(NC2COC2)nc1
Reaction #626762
6-(oxetan-3-ylamino)nicotinonitrile
Ausbeute 25.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_10
Cc1ccc2nc(N3CCS(=O)(=O)c4ccccc4C3)cc(NC3COC3)c2c1
Reaction #627218
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_10
CC(C)(O)C#Cc1cc2c(cc1F)OCCn1c-2nc(C(N)=O)c1CO
Reaction #662335
9-fluoro-3-(hydroxymethyl)-10-(3-hydroxy-3-methyl-but-1-ynyl)-5,6-dihydroimidazo[1,2-d][1,4]benzoxazepine-2-carboxamide
Ausbeute 20.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_05
CC(C)(O)C#Cc1cc2c(cc1F)OCCn1c-2nc(C(N)=O)c1CO
Reaction #662336
9-fluoro-3-(hydroxymethyl)-10-(3-hydroxy-3-methyl-but-1-ynyl)-5,6-dihydroimidazo[1,2-d][1,4]benzoxazepine-2-carboxamide
Ausbeute 6.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_05
CC(C)(O)C#Cc1ccc2c(c1)-c1nc(C(N)=O)c(CNC3COC3)n1CCO2
Reaction #662433
titled compound
Ausbeute 17.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_05
NS(=O)(=O)NC1COC1
Reaction #677138
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_01
O=C(N1CCOCC1)N1CC(c2ccc(C(F)(F)F)cc2)CC(c2nc(NC3COC3)no2)C1
Reaction #748455
Morpholin-4-yl{3-[3-(oxetan-3-ylamino)-1,2,4-oxadiazol-5-yl]-5-[4-(trifluoromethyl)phenyl]-piperidin-1-yl}methanone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_12
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