4-benzyloxyphenylhydrazine hydrochloride

O=C1CCCc2[nH]c3ccc(OCc4ccccc4)cc3c21
Reaction #4478
title compound
Rendement 38.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
c1ccc(COc2ccc(-n3nccc3-c3ccccn3)cc2)cc1
Reaction #62152
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CCOC(=O)C(C)C1CCc2c([nH]c3ccc(OCc4ccccc4)cc23)C1
Reaction #65987
red colored crude product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
CCOC(=O)C=C1CCc2c1[nH]c1ccc(OCc3ccccc3)cc21
Reaction #91087
Ethyl 2-(7-(Benzyloxy)-1,2-dihydrocyclopenta[b]indol-3(4H)-ylidene)acetate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
Cc1[nH]c2ccc(OCc3ccccc3)cc2c1-c1cccc(Cl)c1
Reaction #95098
5-Benzyloxy-3-(3-chloro-phenyl)-2-methyl-1H-indole
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_08
Cl.NCCOc1ccc(-c2cc(C(F)(F)F)nn2-c2ccc(OCc3ccccc3)cc2)cc1
Reaction #438403
title compound
Rendement 87.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_02
CN(C)C1CCc2[nH]c3ccc(OCc4ccccc4)cc3c2C1
Reaction #452434
title compound
Rendement 24.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_10
CN(C)C1CCc2[nH]c3ccc(OCc4ccccc4)cc3c2C1
Reaction #528113
title compound
Rendement 24.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_05
CN(C)C1CCc2[nH]c3ccc(OCc4ccccc4)cc3c2C1
Reaction #528123
title compound
Rendement 24.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_05
CCOC(=O)C(C)C1CCc2c([nH]c3ccc(OCc4ccccc4)cc23)C1
Reaction #571440
red colored crude product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_07
CCOC(=O)C=C1CCc2c1[nH]c1ccc(OCc3ccccc3)cc21
Reaction #621460
Ethyl 2-(7-(Benzyloxy)-1,2-dihydrocyclopenta[b]indol-3(4H)-ylidene)acetate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_10
CCc1nn(-c2ccc(OCc3ccccc3)cc2)c2ncccc12
Reaction #659355
title compound
Rendement 25.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_05
COc1ccc2c(c1)-c1c(c(C)nn1-c1ccc(OCc3ccccc3)cc1)CC2
Reaction #685951
desired product
Rendement 32.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_03
COc1ccc(-c2c(C)nn(-c3ccc(OCc4ccccc4)cc3)c2C)cc1
Reaction #685968
pyrazole
Rendement 61.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_03
CN(C)C1CCc2[nH]c3ccc(OCc4ccccc4)cc3c2C1
Reaction #697857
title compound
Rendement 24.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_12
c1ccc(COc2ccc3[nH]c4c(c3c2)COc2ccccc2-4)cc1
Reaction #711652
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_04
c1ccc(COc2ccc3[nH]c4c(c3c2)COc2ccccc2-4)cc1
Reaction #729935
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_04
CC(C)(C)c1cc(N)n(-c2ccc(OCc3ccccc3)cc2)n1
Reaction #745029
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_12
CCOC(=O)C=C1CCc2c1[nH]c1ccc(OCc3ccccc3)cc21
Reaction #794960
Ethyl 2-(7-(Benzyloxy)-1,2-dihydrocyclopenta[b]indol-3(4H)-ylidene)acetate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_11
CN(C)C1CCc2[nH]c3ccc(OCc4ccccc4)cc3c2C1
Reaction #813267
title compound
Rendement 24.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_01
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