DIAD

CC(C)(C)OC(=O)C(C)(C)Sc1nc(CCOc2ccc(Br)cn2)cs1
Reaction #391445
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CCN(CC)CCCOc1ccc(-c2ccc3c(c2)c2cc(Cl)cnc2n3S(=O)(=O)c2ccccc2)cc1
Reaction #428472
3-(4-(3-chloro-9-(benzenesulfonyl)-9H-pyrido[2,3-b]indol-6-yl)phenoxy)-N,N-diethylpropan-1-amine
收率 51.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
CCOC(=O)C(Cc1ccc(OCCN2COc3ccccc3C2=O)cc1)OCC
Reaction #453534
title compound
收率 76.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_10
CCOC(=O)C(Cc1ccc(OCCN2COc3ccccc3C2=O)cc1)OCC
Reaction #520161
title compound
收率 76.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_12
Cc1nc(OC(c2ccc(F)cc2)C(F)(F)F)c(Br)cc1[N+](=O)[O-]
Reaction #607445
title compound
收率 62.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_05
Cc1nc(OC(c2ccc(C(F)(F)F)cc2)C(F)(F)F)c(Br)cc1[N+](=O)[O-]
Reaction #607447
title compound
收率 41.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_05
CCOCc1nc2cnc3cc(OC4CCN(C(=O)OC(C)(C)C)CC4)ccc3c2n1CC1COC(C)(C)O1
Reaction #628069
tert-butyl 4-{[1-[(2,2-dimethyl-1,3-dioxolan-4-yl)methyl]-2-(ethoxymethyl)-1H-imidazo[4,5-c]quinolin-7-yl]oxy}piperidine-1-carboxylate
收率 76.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_10
COCC(C)Oc1ccc2c(c1)c(-c1cc3cccnc3n1S(=O)(=O)c1ccc(C)cc1)cn2C
Reaction #636232
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_05
CC(C)(C)OC(=O)C(C)(C)Sc1nc(CCOc2ccc(Br)cc2)cs1
Reaction #1001486
title compound
收率 74.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_09
CC(C)(C)OC(=O)C(C)(C)Sc1nc(CCOc2ccc(Br)cn2)cs1
Reaction #1001500
title compound
收率 57.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_09
COc1ccc(Nc2nccc(-c3ccc(C(=O)NC(C)c4ccccc4)s3)n2)cc1OCCN(C)C
Reaction #1099377
5-{2-[3-(2-Dimethylamino-ethoxy)-4-methoxy-phenylamino]-pyrimidin-4-yl}-thiophene-2-carboxylic acid (1-phenyl-ethyl)-amide
收率 1.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_07
Cc1cnc(-c2cccc(Cn3nc(-c4cccc(C#N)c4)ccc3=O)c2)nc1
Reaction #1495574
3-{1-[3-(5-methylpyrimidin-2-yl)benzyl]-6-oxo-1,6-dihydropyridazin-3-yl}benzonitrile
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_12
COc1ccc(Nc2nccc(-c3ccc(C(=O)NC(C)c4ccccc4)s3)n2)cc1OCCN(C)C
Reaction #1803592
5-{2-[3-(2-Dimethylamino-ethoxy)-4-methoxy-phenylamino]-pyrimidin-4-yl}-thiophene-2-carboxylic acid (1-phenyl-ethyl)-amide
收率 1.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_09
COCC(C)Oc1ccc2c(c1)c(-c1cc3cccnc3n1S(=O)(=O)c1ccc(C)cc1)cn2C
Reaction #1852782
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_06
COCC(C)Oc1ccc2c(c1)c(-c1cc3cccnc3n1S(=O)(=O)c1ccc(C)cc1)cn2C
Reaction #1922401
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_08
CC(C)(C)OC(=O)C(C)(C)Sc1nc(CCOc2ccc(Br)cc2)cs1
Reaction #2223294
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (4/10)
CCOCc1nc2cnc3cc(OC4CCN(C(=O)OC(C)(C)C)CC4)ccc3c2n1CC1COC(C)(C)O1
Reaction #2290745
tert-butyl 4-{[1-[(2,2-dimethyl-1,3-dioxolan-4-yl)methyl]-2-(ethoxymethyl)-1H-imidazo[4,5-c]quinolin-7-yl]oxy}piperidine-1-carboxylate
收率 76.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_06
CCOC(=O)C(Cc1ccc(OCCN2COc3ccccc3C2=O)cc1)OCC
Reaction #2357631
title compound
收率 76.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_12