An 47 Reaktionen beteiligt

165913

CC(C)(C)c1cc([N+](=O)[O-])c(C(=O)N2CCNC(=O)C2(C)C)[nH]1
Reaction #47211
4-(2-tert-butyl-4-nitro-1H-pyrrole-5-carbonyl)-3,3-dimethylpiperazin-2-one
Ausbeute 53.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(C)(C)c1cc(C(=O)N2CCNC(=O)C2(C)C)c([N+](=O)[O-])[nH]1
Reaction #47214
4-(2-tert-butyl-5-nitro-1H-pyrrole-4-carbonyl)-3,3-dimethylpiperazin-2-one
Ausbeute 49.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC1(C)NCCNC1=O
Reaction #71414
3,3-dimethyl-piperazin-2-one
Ausbeute 65.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CN1CCNC(=O)C1(C)C
Reaction #71415
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
COc1ccc(CN2CCNC(=O)C2(C)C)cc1
Reaction #71417
title compound
Ausbeute 55.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CC1(C)NCCNC1=O
Reaction #71418
title compound
Ausbeute 68.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CC(C)(C)OC(=O)Nc1ccc(CN2CCNC(=O)C2(C)C)cn1
Reaction #71422
title compound
Ausbeute 67.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CCc1nc2ccccc2n1-c1nc(N2CCOCC2)c2nc(CN3CCNC(=O)C3(C)C)n(C)c2n1
Reaction #230377
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CN1CCNC(=O)C1(C)C
Reaction #406162
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CC1(C)C(=O)NCCN1CC1CN(Cc2ccccc2)CCN1Cc1ccccc1
Reaction #406163
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CC1(C)NCCNC1=O
Reaction #586395
3,3-dimethylpiperazin-2-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_08
CN1CCNC(=O)C1(C)C
Reaction #586396
title compound
Ausbeute 73.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_08
CC1(C)NCCNC1=O
Reaction #587837
3,3-dimethylpiperazin-2-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_08
CC1(C)NCCNC1=O
Reaction #744785
3,3-dimethylpiperazin-2-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_12
CN1CCNC(=O)C1(C)C
Reaction #744786
title compound
Ausbeute 73.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_12
CC(C)(C)c1cc(C(=O)N2CCNC(=O)C2(C)C)c([N+](=O)[O-])[nH]1
Reaction #909937
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
CC(C)(C)c1cc([N+](=O)[O-])c(C(=O)N2CCNC(=O)C2(C)C)[nH]1
Reaction #1030083
DOI: 10.1039/C8SC04228DValidation data from https://doi.org/10.1039/C8SC04228D
CC(C)(C)OC(=O)Nc1ccc(CN2CCNC(=O)C2(C)C)cn1
Reaction #1037161
DOI: 10.1039/C8SC04228DValidation data from https://doi.org/10.1039/C8SC04228D
CC1(C)NCCNC1=O
Reaction #1134288
3,3-dimethylpiperazin-2-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_10
CC1(C)NCCNC1=O
Reaction #1277004
3,3-dimethyl-piperazin-2-one
Ausbeute 65.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_03
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