phenylazide

CCOC(=O)c1nnn(-c2ccccc2)c1N
Reaction #55964
Ethyl 5-amino-1-phenyl-1,2,3-triazole-4-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_09
O=C(Nc1ccccc1)Nc1ccccc1
Reaction #487499
Diphenylurea
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_06
CC(=O)Nc1ccccc1
Reaction #487500
Acetoanilide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_06
COc1c(Cc2c[nH]nn2)ccn(-c2ccccc2)c1=O
Reaction #626707
white solid 151a
収率 92.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_10
COc1cc(OCc2cn(-c3ccccc3)nn2)c2cc(-c3cn4nc(OC)sc4n3)oc2c1
Reaction #712295
title material
収率 49.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_04
COc1cc(OCc2cnnn2-c2ccccc2)c2cc(-c3cn4nc(OC)sc4n3)oc2c1
Reaction #712296
title material
収率 14.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_04
OCc1cn(-c2ccccc2)nn1
Reaction #715858
desired product 7
収率 35.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_04
C1=CCCCCCC1
Reaction #762890
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
c1ccc(-n2cc(-c3ccco3)nn2)cc1
Reaction #792185
4-(furan-2-yl)-1-phenyl-1H-1,2,3-triazole
収率 62.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_11
c1ccc(-n2cc(-c3cccs3)nn2)cc1
Reaction #792187
1-phenyl-4-(thiophen-2-yl)-1H-1,2,3-triazole
収率 47533.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_11
—
Reaction #814272
solid
収率 27.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_01
CC[C@H]1CN(C(=O)OC(C)(C)C)C[C@H]1Nc1c(C(N)=O)cnn2cc(-c3cn(-c4ccccc4)nn3)cc12
Reaction #964988
title compound
収率 44.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_03
c1ccc(-n2ccnn2)cc1
Reaction #1076343
1-phenyl triazole
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_10
O=c1nc2n(-c3ccccc3)[nH]nc-2c2ccccc12
Reaction #1104820
3-phenyl-1,2,3-triazolo[4,5-c]isoquinolin-5-one
収率 64.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_11
O=C(O)c1nnn(-c2ccccc2)c1COCc1ccccc1
Reaction #1271410
product
収率 86.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_03
COCCCCc1c(C(=O)O)nnn1-c1ccccc1
Reaction #1271445
product
収率 52.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_03
O=C(O)c1nnn(-c2ccccc2)c1CCc1ccccc1
Reaction #1271449
product
収率 32.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_03
O=C(O)c1nnn(-c2ccccc2)c1COCc1ccccc1
Reaction #1347235
product
収率 86.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_06
COCCCCc1c(C(=O)O)nnn1-c1ccccc1
Reaction #1347272
product
収率 52.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_06
O=C(O)c1nnn(-c2ccccc2)c1CCc1ccccc1
Reaction #1347276
product
収率 32.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_06
1 ページ次のページ