5-[[3,5-bis(1,1-dimethylethyl) -4-hydroxyphenyl]methylene]-4-thiazolidinone

CC(C)c1cc(C=C2SCN(C)C2=O)cc(C(C)C)c1O
Reaction #3031
5-[[3,5-bis(1-methylethyl)-4-hydroxyphenyl]methylene]-3-methyl-4-thiazolidinone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCN1CSC(=Cc2cc(C(C)(C)C)c(O)c(C(C)(C)C)c2)C1=O
Reaction #3037
desired title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)(C)c1cc(C=C2SCN(CC#N)C2=O)cc(C(C)(C)C)c1O
Reaction #3041
desired title product
Выход 40.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CSCCN1CSC(=Cc2cc(C(C)(C)C)c(O)c(C(C)(C)C)c2)C1=O
Reaction #191541
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)(C)c1cc(C=C2SCNC2=O)cc(C(C)(C)C)c1O
Reaction #554371
Compound B
Выход 7.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1992_10
CSCCN1CSC(=Cc2cc(C(C)(C)C)c(O)c(C(C)(C)C)c2)C1=O
Reaction #554372
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1992_10
CC(C)(C)c1cc(C=C2SCN(CC#N)C2=O)cc(C(C)(C)C)c1O
Reaction #554378
desired title product
Выход 40.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1992_10
CC(C)(C)c1cc(C=C2SCNC2=O)cc(C(C)(C)C)c1O
Reaction #924082
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
CC(C)(C)c1cc(C=C2SCN(C(N)=O)C2=O)cc(C(C)(C)C)c1O
Reaction #1196472
objective compound
Выход 69.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1994_06
CC(C)(C)c1cc(C=C2SCN(C(N)=O)C2=O)cc(C(C)(C)C)c1O
Reaction #1196538
objective compound
Выход 69.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1994_06
CCN1CSC(=Cc2cc(C(C)(C)C)c(O)c(C(C)(C)C)c2)C1=O
Reaction #1217357
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (7/10)
CC(C)(C)c1cc(C=C2SCN(CC#N)C2=O)cc(C(C)(C)C)c1O
Reaction #1224345
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (7/10)
CSCCN1CSC(=Cc2cc(C(C)(C)C)c(O)c(C(C)(C)C)c2)C1=O
Reaction #1795418
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1994_10
CCN1CSC(=Cc2cc(C(C)(C)C)c(O)c(C(C)(C)C)c2)C1=O
Reaction #1795422
desired title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1994_10
CC(C)(C)c1cc(C=C2SCN(CC#N)C2=O)cc(C(C)(C)C)c1O
Reaction #1795427
desired title product
Выход 40.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1994_10
CC(C)(C)c1cc(C=C2SCN(C(N)=O)C2=O)cc(C(C)(C)C)c1O
Reaction #2238754
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (4/10)
CC(C)(C)c1cc(C=C2SCNC2=O)cc(C(C)(C)C)c1O
Reaction #2382243
Compound B
Выход 7.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_11
CSCCN1CSC(=Cc2cc(C(C)(C)C)c(O)c(C(C)(C)C)c2)C1=O
Reaction #2382244
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_11
CCN1CSC(=Cc2cc(C(C)(C)C)c(O)c(C(C)(C)C)c2)C1=O
Reaction #2382248
desired title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_11
CC(C)(C)c1cc(C=C2SCN(CC#N)C2=O)cc(C(C)(C)C)c1O
Reaction #2382251
desired title product
Выход 40.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_11