2-methyl-2-butanol

CCn1ncc(C(=O)c2cc(C)c3c(c2C)C(C)(C)CCS3(=O)=O)c1O
Reaction #1164
4,4,5,8-tetramethyl-6-(1-ethyl-5-hydroxypyrazol-4-yl)carbonylthiochroman-1,1-dioxide
Yield 62.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCC(C)(C)O[Si](OC)(OC)C1CCCC1
Reaction #6544
tert-amyloxy cyclopentyl dimethoxysilane
Yield 82.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CCCCCCCc1ccccc1
Reaction #42165
1-phenylheptane
Yield 89.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COc1c(-c2ccc3cc(NS(C)(=O)=O)ccc3c2)cc(-n2ccc(=O)[nH]c2=O)cc1C(C)(C)C
Reaction #86681
title compound
Yield 73.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
COc1c(-c2ccc3cc(NS(C)(=O)=O)ccc3c2)cc(-n2ccc(=O)[nH]c2=O)cc1C(C)(C)C
Reaction #86684
N-(6-(3-tert-butyl-5-(2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-2-methoxyphenyl)naphthalen-2-yl)methanesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
COc1c(-c2ccc3cc(NS(C)(=O)=O)ccc3c2)cc(-n2ccc(=O)[nH]c2=O)cc1C(C)(C)C
Reaction #86689
titled compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
COc1c(-c2ccc3cc(NS(C)(=O)=O)ccc3c2)cc(-n2ccc(=O)[nH]c2=O)cc1C(C)(C)C
Reaction #86690
titled compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
FC(F)(F)c1ccc(Nc2nc(N3CCOCC3)nc3sc(Cc4c(Cl)cccc4Cl)nc23)cc1
Reaction #88479
title compound
Yield 77.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
—
Reaction #161648
material
Yield 97.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=C(OCc1ccccc1)N1CCC(n2c(=O)[nH]c3ncccc32)CC1
Reaction #161672
benzyl 4-(2-oxo-2,3-dihydro-imidazo[4,5-b]pyridin-1-yl)-piperidine-1-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Cc1ccc(NS(C)(=O)=O)cc1
Reaction #166170
N-p-tolylmethanesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=C1NC(c2cccs2)=C2C(=O)NC(c3cccs3)=C12
Reaction #171154
3,6-bis(thiophen-2-yl)-2H,5H-pyrrolo[3,4-c]pyrrole-1,4-dione
Yield 82.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Cc1ccc(C(C)(C)C)cc1Nc1cc(C(=O)N(C)C)cc(N2CCC(n3ccnc3)CC2)n1
Reaction #173648
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
OCCc1nccn1Cc1coc(-c2ccc(OCc3ccccc3)cc2)n1
Reaction #182610
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(=O)CC(C)(C)C(Cl)CC(Cl)(Cl)Cl
Reaction #189197
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)(O)c1cc(F)c(-c2nc(C(N)=O)c(Nc3cccc(C(CO)N4CCOCC4)n3)s2)c(F)c1
Reaction #189980
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCn1ncc(C(=O)c2cc(F)c3c(c2C)C(OC)CC(C)S3(=O)=O)c1O
Reaction #216616
8-fluoro-4-methoxy-2,5-dimethyl-6-(1-ethyl-5-hydroxypyrazol-4-yl)carbonylthiochroman-1,1-dioxide
Yield 76.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_11
CC(=O)N1CC(O)CC1C(=O)N1CCCNCC1
Reaction #226177
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(C)(O)c1ccc(-c2nc(C(N)=O)c(Nc3ccc(S(C)(=O)=O)cn3)s2)cc1
Reaction #235615
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(C)(O)c1cc(F)c(-c2cc(C(N)=O)c(Nc3ccc4c(n3)CN(CCO)C4=O)s2)c(F)c1
Reaction #244709
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
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