dihexylamine

CCCCCCN(CCCCCC)c1ccc2nc3ccc(N(CCC)CCC)cc3[s+]c2c1.[I-]
Reaction #42648
3-(N,N-dihexylamino)-7-(N,N-dipropylamino)-phenothiazin-5-ium iodide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCCCCCN(CCCCCC)C1=NS(=O)(=O)N=C1OCC
Reaction #46328
title intermediate
Yield 72.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCCCCCN(CCCCCC)c1ccc([N+](=O)[O-])cc1F
Reaction #84424
title compound
Yield 86.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CCCCCCN(CCCCCC)c1ccc([N+](=O)[O-])cc1C#N
Reaction #84483
title compound
Yield 87.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CCCCCCN(CCCCCC)S(=O)(=O)c1ccc2nc(C)sc2c1
Reaction #171961
Compound 20
Yield 97.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCCCCCN(CCCCCC)C(=O)c1c(O)c2ccccc2n(Cc2ccccc2)c1=O
Reaction #191481
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCCCCN(CCCCCC)Cc1nc(-c2ncn3c2C2CCN2C(=O)c2c(Cl)cccc2-3)no1
Reaction #384281
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CCCCCCN(CCCCCC)C(=O)c1cc2ccccc2[nH]c1=O
Reaction #397163
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CCCCCCN(CCCCCC)S(=O)(=O)c1ccc2nc(C)sc2c1
Reaction #496884
Compound 20
Yield 97.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_06
CCCCCCN(CCCCCC)c1cc(C)cc(O)c1
Reaction #516688
1-di-n-hexylamino-3-methyl-5-hydroxybenzene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_11
CCCCCCN(CCCCCC)c1nc(Cl)nc(Cl)n1
Reaction #582219
2,4-dichloro-6-dihexylamino-1,3,5-triazine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_05
CCCCCCN(CCCCCC)C1=NS(=O)(=O)N=C1OCC
Reaction #582221
4-(N,N-di-n-hexylamino)-3-ethoxy-1,1-dioxo-1,2,5-thiadiazole
Yield 72.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_05
CCCCCCN(CCCCCC)c1ccc2nc3ccc(N(CCC)CCC)cc3[s+]c2c1.[I-]
Reaction #692689
3-(N,N-dihexylamino)-7-(N,N-dipropylamino)-phenothiazin-5-ium iodide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_03
CCCCCCN(CCCCCC)C(=O)C1CC(=O)c2ccccc2S1
Reaction #738761
N,N-dihexyl-(4-oxo-thiochroman-2-yl)-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_08
CCCCCCN(CCCCCC)C(=O)[C@H](C)N(C(=O)OC(C)(C)C)c1ccccc1C#N
Reaction #738764
N-t-butoxycarbonyl-(2-cyanophenyl)alanine dihexylamide
Yield 79.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_08
CCCCCCN(CCCCCC)C(=O)c1nc2ccccc2n(Cc2ccccc2)c1=O
Reaction #931702
N,N-dihexyl-1-benzyl-1,2-dihydro-2-oxoquinoxaline-3-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_04
CCCCCCN(CCCCCC)C(=O)c1cc2ccccc2[nH]c1=O
Reaction #931703
N,N-dihexyl-1,2-dihydro-2-oxoquinoline-3-carboxamide
Yield 75.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_04
CCCCCCN(CCCCCC)C(=O)c1c(O)c2ccccc2n(Cc2ccccc2)c1=O
Reaction #931706
N,N-dihexyl-1-benzyl-4-hydroxy-1,2-dihydro-2-oxoquinoline-3-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_04
CCCCCCN(CCCCCC)CON(Cc1ccccc1)Cc1ccccc1
Reaction #932463
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_07
CCCCCCC/C=C/C(=O)N(CCCCCC)CCCCCC
Reaction #966075
aimed compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_03
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