Involved in 174 reactions

CCCCNC

CCCCN(C)Cc1ccc(C(=O)OC)s1
Reaction #42386
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCCCN(C)Cc1cc(C)cc(C(=O)OC)c1
Reaction #42389
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCCCN(C)Cc1cc(Br)cc(C(=O)OC)c1
Reaction #42391
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCCCN(C)Cc1cc(C(=O)OC)cc(-c2ncco2)c1
Reaction #42397
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCCCN(C)c1nccc2ccc(Br)cc12
Reaction #42540
7-bromo-N-butyl-N-methylisoquinolin-1-amine
Yield 161.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCCCN(C)C(=O)c1cc(I)cc(C(=O)OC)c1
Reaction #42575
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCCCN(C)CCCCCOc1c(OC)ccc2c(Nc3c(Cl)cncc3Cl)cc(=O)oc12
Reaction #48987
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCCCN(C)C(=O)c1cccc(C(=O)O)c1
Reaction #49219
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCCCN(C)C(=O)c1cccc(C(=O)N[C@@H](Cc2cc(F)cc(F)c2)[C@H](O)[C@H]2C[C@@H](OCCC)CN2)c1
Reaction #49233
title compound
Yield 80.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCCCN(C)C(=O)c1cc(C)cc(C(=O)N[C@@H](Cc2cc(F)cc(F)c2)[C@H](O)[C@H]2C[C@@H](OCCC)CN2)c1
Reaction #49240
title compound
Yield 85.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCCCc1nn(-c2cc(C(=O)N(C)CCCC)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1
Reaction #64549
title compound
Yield 36.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
CCCCN(C)C(C)(OC)OC
Reaction #64598
N-butyl-N-methylacetamide dimethyl acetal
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
CCCCN(C)c1ncc(C(=O)OCCC(C)=C(F)F)c(C)n1
Reaction #185249
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCCc1nn(-c2cc(C(=O)N(C)CCCC)ccc2Cl)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(=O)c2ccccc2Cl)cc1
Reaction #202929
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCCN(C)Cc1cc(C(=O)OC)cc(-c2ncco2)c1
Reaction #204112
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCCN(C)CCc1ccc(Nc2ncc3c(n2)-c2ccccc2C(c2ccccc2C(F)(F)F)C3)cc1
Reaction #224599
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCCCN(C)C(=O)c1ccc2ccccc2c1
Reaction #226945
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCCCN(C)C(=O)CCCCCCCBr
Reaction #246626
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCCCN(C)S(=O)(=O)CCCCCCl
Reaction #249833
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCCCN(C)Cc1ccc(C(=O)OC)s1
Reaction #266921
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
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