ethoxycarbonyl isothiocyanate

CCOC(=O)NC(=S)CNc1ccc(C(=O)OC)c(S(=O)(=O)NC(C)(C)C)c1
Reaction #1095
N-tert-butyl-5-[N-(ethoxycarbonylaminothiocarbonyl)methylamino]-2-methoxycarbonylbenzenesulfonamide
収率 75.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOC(=O)NC(=Nc1cccnc1NC1CCCCC1)N(CC)CC
Reaction #11382
Ethyl {[2-(cyclohexylamino)-3-pyridyl]imino}(diethylamino)methylcarbamate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCOC(=O)NC(=S)Nc1ncccc1Br
Reaction #86040
ethyl [(3-bromopyridin-2-yl) carbamothioyl]carbamate
収率 100.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
COC(=O)c1ccn2nc(N)nc2c1
Reaction #88424
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CCCCc1cn(C(C)(C)C)s/c1=N\C(=O)OCC
Reaction #163456
title compound
収率 92.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCCCc1cn(C(C)(C)C)s/c1=N\C(=O)OCC
Reaction #163474
title compound
収率 67.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCCCc1cn(C(C)(C)C(F)(F)F)s/c1=N\C(=O)OCC
Reaction #163486
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCOC(=O)NC(=S)Nc1ccc(C(=O)OC(C)(C)C)cc1
Reaction #176550
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(=O)NC(=S)Nc1ccc(Oc2cc(NC(=O)c3cccc(C(C)(C)C#N)c3)ccc2C)cn1
Reaction #203188
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(=O)NC(=S)Nc1ncc(C2CC2)cc1Br
Reaction #228711
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCCCOC(=S)NC(=O)OCC
Reaction #253495
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCOC(=O)NC(=S)Nc1ccc(Oc2ccc(C)c(NC(=O)c3cc(C)nn3C)c2)cn1
Reaction #265947
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCOC(=O)NC(=S)OCc1ccccc1
Reaction #269268
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCOC(=O)NC(=S)N(Cc1ccc2c(c1)Cc1ccccc1-2)c1ccc(C(=O)OC)cc1
Reaction #273476
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCOC(=O)NC(=S)N1CCOCC1
Reaction #282717
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCOC(=O)NC(=S)Nc1ccc(Oc2cccc(NC(=O)c3cc(C)nn3C)c2)cn1
Reaction #289166
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCOC(=O)NC(=S)Nc1ccc(OC)cn1
Reaction #298756
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCOC(=O)NC(=S)Nc1ccc(Br)cn1
Reaction #328198
ethyl {[(5-bromopyridin-2-yl)amino]carbonothioyl}carbamate
収率 70.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
C=C(NC(=O)OCC)Nc1ncc(-c2ccc3c(c2)CN(c2ncnc4c2CC(C)(C)CC4)CCO3)cc1N
Reaction #328410
ethyl [1-({3-amino-5-[4-(6,6-dimethyl-5,6,7,8-tetrahydroquinazolin-4-yl)-2,3,4,5-tetrahydro-1,4-benzoxazepin-7-yl]pyridine-2-yl}amino)ethenyl]carbamate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
CCOC(=O)NC(N)=S.COc1ccc(N)nc1
Reaction #337200
5-methoxypyridin-2-amine ethoxycarbonyl thiourea
収率 201.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_01
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