4-tert-butylbenzoyl chloride

CC(C)(C)c1ccc(C(=O)NCCCSc2ccncc2)cc1.Cl
Reaction #6203
desired compound
Ausbeute 88.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
COC(=O)c1ccc([N+](=O)[O-])cc1NC(=O)c1ccc(C(C)(C)C)cc1
Reaction #57938
2-(4-tert-butyl-benzoylamino)-4-nitro-benzoic acid methyl ester
Ausbeute 60.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CCOC(=O)c1cnc(NC(=O)c2ccc(C(C)(C)C)cc2)s1
Reaction #77422
amide
Ausbeute 88.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
CC(C)(C)c1ccc(C(=O)NCc2ccc3c(c2)C(=O)N(C2CCC(=O)NC2=O)C3=O)cc1
Reaction #91685
4-tert-butyl-N-((2-(2,6-dioxopiperidin-3-yl)-1,3-dioxoisoindolin-5-yl)methyl)benzamide
Ausbeute 80.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CC(C)(C)c1ccc(C(=O)NCc2ccc3c(c2)CN(C2CCC(=O)NC2=O)C3=O)cc1
Reaction #91718
4-tert-butyl-N-[2-(2,6-dioxo-piperidin-3-yl)-1-oxo-2,3-dihydro-1H-isoindol-5-ylmethyl]-benzamide
Ausbeute 92.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CC(C)(CO)NC(=O)c1ccc(C(C)(C)C)cc1
Reaction #155642
title compound
Ausbeute 105.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
—
Reaction #158112
solid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC(C)(C)c1ccc(C(=O)Nc2cccc(S(=O)(=O)O)c2)cc1
Reaction #166279
3-(4-tert-butylbenzamido)benzenesulfonic acid
Ausbeute 63.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCOC(=NC(=O)c1ccc(C(C)(C)C)cc1)N1Cc2ccccc2-c2ccccc2C1
Reaction #188579
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(Cc1ccc(OCCc2ccc(NC(=O)c3ccc(C(C)(C)C)cc3)cc2)cc1)C(=O)O
Reaction #188850
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(=O)c1ccc(Nc2nc(-c3cccc(NC(=O)c4ccc(C(C)(C)C)cc4)c3)cn3ccnc23)cc1
Reaction #221159
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(C)(C)c1ccc(C(=O)Nc2cc[nH]c(=O)n2)cc1
Reaction #225600
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(C)(C)c1ccc(C(=O)Nc2cccc(-c3cn4ccnc4c(Nc4ccc5ncsc5c4)n3)c2)cc1
Reaction #229342
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(C)(C)c1ccc(C(=O)Nc2cccc(Br)c2Br)cc1
Reaction #229546
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCCCc1ccc(C#Cc2ccc(CN(C(=O)c3ccc(C(C)(C)C)cc3)c3ccc4c(c3)C(=O)OC(C)(C)O4)cc2)cc1
Reaction #231135
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cc1c(NC(=O)c2ccc(C(C)(C)C)cc2)cccc1-c1cn2ccnc2c(Nc2ccc(C#N)cc2)n1
Reaction #235078
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(C)(C)c1ccc(C(=O)c2ccc3n2Cc2ccccc2N(C(=O)c2ccc(C4CCCCC4)cc2)C3)cc1
Reaction #241249
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC(C)(CO)NC(=O)c1ccc(C(C)(C)C)cc1
Reaction #247012
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cc1c(NC(=O)c2ccc(C(C)(C)C)cc2)cccc1-c1cc(Br)c(=O)n(C)c1
Reaction #249917
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cl
Reaction #252624
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
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