4-(3,4-diaminophenyl)benzene-1,2-diamine

C#C.C#C.c1ccc2[nH]cnc2c1.c1ccc2[nH]cnc2c1
Reaction #1814
benzobisimidazole Divinylene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
N=C1CCCCC1.N=C1CCCCC1.N=C1CCCCC1.N=C1CCCCC1.Nc1ccc(-c2ccc(N)c(N)c2)cc1N
Reaction #543544
3,3′-diaminobenzidine tetracyclohexanimine
Yield 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_03
CC(C)=N.CC(C)=N.CC(C)=N.CC(C)=N.Nc1ccc(-c2ccc(N)c(N)c2)cc1N
Reaction #543545
3,3′-diaminobenzidine tetraisopropanimine
Yield 76.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_03
CC(C)=N.Nc1ccc(-c2ccc(N)c(N)c2)cc1N
Reaction #543546
3,3′-diaminobenzidine monoisopropanimine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_03
Nc1ccc(-c2nc3cc(-c4ccc5nc(-c6ccc(N)cc6)[nH]c5c4)ccc3[nH]2)cc1
Reaction #715754
product
Yield 97.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_04
Oc1ccc(-c2nc3cc(-c4ccc5[nH]c(-c6ccc(O)cc6)nc5c4)ccc3[nH]2)cc1
Reaction #715755
product
Yield 6.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_04
Nc1ccc(-c2nc3ccc(-c4ccc(N)c(N)c4)cc3[nH]2)cc1
Reaction #715760
4-(2-(4-Aminophenyl)-1H-benzo[d]imidazol-6-yl)benzene-1,2-diamine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_04
COc1ccc(-c2nc3ccc(-c4ccc(N)c(N)c4)cc3[nH]2)cc1
Reaction #715762
4-(2-(4-Methoxyphenyl)-1H-benzo[d]imidazol-6-yl)benzene-1,2-diamine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_04
Oc1ccc(-c2nc3cc(-c4ccc5[nH]c(-c6ccc(O)cc6)nc5c4)ccc3[nH]2)cc1
Reaction #960523
product
Yield 6.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_03
Nc1ccc(-c2nc3ccc(-c4ccc(N)c(N)c4)cc3[nH]2)cc1
Reaction #960528
4-(2-(4-Aminophenyl)-1H-benzo[d]imidazol-6-yl)benzene-1,2-diamine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_03
COc1ccc(-c2nc3ccc(-c4ccc(N)c(N)c4)cc3[nH]2)cc1
Reaction #960530
4-(2-(4-Methoxyphenyl)-1H-benzo[d]imidazol-6-yl)benzene-1,2-diamine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_03
Nc1ccc(-c2ccc(N)c(N)c2)cc1N
Reaction #1760252
3,3′-diaminobenzidine
Yield 74.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_08
Nc1ccc(-c2ccc(N)c(N)c2)cc1N
Reaction #1760253
3,3′-diaminobenzidine
Yield 70.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_08
Nc1ccc(-c2ccc(N)c(N)c2)cc1N
Reaction #1760254
3,3′-diaminobenzidine
Yield 69.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_08
Nc1ccc(-c2ccc(N)c(N)c2)cc1N
Reaction #1907154
3,3′,4,4′-tetraaminobiphenyl
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_10
Nc1ccc(-c2ccc(N)c(N)c2)cc1N
Reaction #1907155
3,3′,4,4′-tetraaminobiphenyl
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_10
OCCOc1ccc(-c2nc3cc(-c4ccc5nc(-c6ccc(OCCO)cc6)[nH]c5c4)ccc3[nH]2)cc1
Reaction #2371340
Compound 260
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_09
O=C(Nc1ccccc1)c1ccc(-c2nc3cc(-c4ccc5nc(-c6ccc(C(=O)Nc7ccccc7)cc6)[nH]c5c4)ccc3[nH]2)cc1
Reaction #2371341
Compound 261
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_09
COc1ccc(/C=C/c2nc3cc(-c4ccc5nc(/C=C/c6ccc(OC)cc6)[nH]c5c4)ccc3[nH]2)cc1
Reaction #2371342
Compound 262
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_09
CN(C)c1ccc(/C=C/c2nc3cc(-c4ccc5nc(/C=C/c6ccc(N(C)C)cc6)[nH]c5c4)ccc3[nH]2)cc1
Reaction #2371343
Compound 264
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_09
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