N-(1,1-dimethylethyl)-1-methyl-1H-pyrrole-3-sulfonamide

COC(=O)c1c(S(=O)(=O)NC(C)(C)C)ccn1C
Reaction #909
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COC(=O)c1c(S(=O)(=O)NC(C)(C)C)ccn1C
Reaction #910
title compound
Ausbeute 55.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CSc1c(S(=O)(=O)NC(C)(C)C)ccn1C
Reaction #912
title compound
Ausbeute 58.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cn1ccc(S(=O)(=O)NC(C)(C)C)c1Br
Reaction #914
title compound
Ausbeute 58.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cn1ccc(S(=O)(=O)NC(C)(C)C)c1C=O
Reaction #916
title compound
Ausbeute 39.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CN(C)S(=O)(=O)c1c(S(N)(=O)=O)c(C(C)(C)C)cn1C
Reaction #919
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CN(C)C(=O)c1c(S(=O)(=O)NC(C)(C)C)ccn1C
Reaction #921
title compound
Ausbeute 50.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COC(=O)c1c(S(=O)(=O)NC(C)(C)C)ccn1C
Reaction #190728
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CSc1c(S(=O)(=O)NC(C)(C)C)ccn1C
Reaction #242697
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cn1ccc(S(=O)(=O)NC(C)(C)C)c1C=O
Reaction #1034099
DOI: 10.1039/C8SC04228DValidation data from https://doi.org/10.1039/C8SC04228D
Cn1ccc(S(=O)(=O)NC(C)(C)C)c1C=O
Reaction #1035477
DOI: 10.1039/C8SC04228DValidation data from https://doi.org/10.1039/C8SC04228D
COC(=O)c1c(S(=O)(=O)NC(C)(C)C)ccn1C
Reaction #1168416
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_12
COC(=O)c1c(S(=O)(=O)NC(C)(C)C)ccn1C
Reaction #1168417
title compound
Ausbeute 55.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_12
CSc1c(S(=O)(=O)NC(C)(C)C)ccn1C
Reaction #1168419
title compound
Ausbeute 58.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_12
Cn1ccc(S(=O)(=O)NC(C)(C)C)c1Br
Reaction #1168421
title compound
Ausbeute 58.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_12
Cn1ccc(S(=O)(=O)NC(C)(C)C)c1C=O
Reaction #1168423
title compound
Ausbeute 39.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_12
CN(C)C(=O)c1c(S(=O)(=O)NC(C)(C)C)ccn1C
Reaction #1168426
title compound
Ausbeute 50.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_12
COC(=O)c1c(S(=O)(=O)NC(C)(C)C)ccn1C
Reaction #2216704
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (4/10)
COC(=O)c1c(S(=O)(=O)NC(C)(C)C)ccn1C
Reaction #2346359
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_12
COC(=O)c1c(S(=O)(=O)NC(C)(C)C)ccn1C
Reaction #2346360
title compound
Ausbeute 55.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_12
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