3-tert butyl-1h-pyrazol-5-amine

CC1Cc2c(ncnc2Oc2ccc3c(ccn3C(=O)Nc3cc(C(C)(C)C)n[nH]3)c2)CN1C(=O)OC(C)(C)C
Reaction #73366
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CC(C)(C)c1cc(N)n(-c2ccc(F)c(O)c2)n1
Reaction #88905
title compound
Ausbeute 70.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CCOC(=O)c1cc(Cl)cc(-n2nc(C(C)(C)C)cc2N)c1
Reaction #88908
title compound
Ausbeute 19.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
Cc1cc(O)cc(-n2nc(C(C)(C)C)cc2N)c1
Reaction #88922
title compound
Ausbeute 49.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CC(C)[Si](Oc1ccc(-n2nc(C(C)(C)C)cc2N)cc1CO)(C(C)C)C(C)C
Reaction #88932
title compound
Ausbeute 15.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CC(C)(C)c1cc(N)n(-c2cc(O)cc(Cl)c2)n1
Reaction #88937
title compound
Ausbeute 62.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CC(C)(C)c1cc(N)n(-c2cn(CCOC3CCCCO3)nc2CO)n1
Reaction #88954
title compound
Ausbeute 63.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CC(C)(C)c1cc(NC(=O)Nc2ccc(-c3cccc4c3CNC4=O)cc2)[nH]n1
Reaction #232257
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC1Cc2c(ncnc2Oc2ccc3c(ccn3C(=O)Nc3cc(C(C)(C)C)n[nH]3)c2)CN1C(=O)OC(C)(C)C
Reaction #537418
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_07
CN(C)/C=N/c1cc(C(C)(C)C)n[nH]1
Reaction #540154
title compound
Ausbeute 99.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_07
CC(C)(C)c1cc(NC(c2ccccc2)(c2ccccc2)c2ccccc2)[nH]n1
Reaction #540163
crude title compound
Ausbeute 77.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_07
CC1Cc2c(ncnc2Oc2ccc3c(ccn3C(=O)Nc3cc(C(C)(C)C)n[nH]3)c2)CN1C(=O)OC(C)(C)C
Reaction #540338
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_07
COc1cccc(OC)c1C(=O)Nc1cc(C(C)(C)C)n[nH]1
Reaction #549548
N-[3-(1,1-dimethylethyl)-1H-pyrazol-5-yl]-2,6-dimethoxybenzamide
Ausbeute 18.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1985_05
COc1ccc(-n2nc(C(C)(C)C)cc2N)cc1OC
Reaction #658268
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_05
Cc1csc(-n2nc(C(C)(C)C)cc2N)c1
Reaction #658269
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_05
CC(C)(C)c1cc(N)n(-c2cnn(CCCOC3CCCCO3)c2)n1
Reaction #718080
title compound
Ausbeute 73.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_04
CC(C)(C)c1cc(N)n(-c2cn(CCOC3CCCCO3)cn2)n1
Reaction #718090
title compound
Ausbeute 35.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_04
COc1cccc(OC)c1C(=O)Nc1cc(C(C)(C)C)n[nH]1
Reaction #768427
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
CC(C)(C)c1cc(N)n(-c2ccc(F)c(O)c2)n1
Reaction #798326
title compound
Ausbeute 70.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_11
CCOC(=O)c1cc(Cl)cc(-n2nc(C(C)(C)C)cc2N)c1
Reaction #798329
title compound
Ausbeute 19.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_11
Seite 1Weiter