benzyl azide

Cc1cc(C)c(-c2nnn(Cc3ccccc3)c2N)c(C)c1
Reaction #10331
solid
수율 61.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CNC(=O)c1cc(Oc2ccc3c(c2)nc(Nc2cccc(-c4cn(Cc5ccccc5)nn4)c2)n3C)ccn1
Reaction #41788
4-{2-(3-(1-Benzyl-1H-[1,2,3]triazol-4-yl)-phenyl amino]-1-methyl-1H-benzoimidazol-5-yloxy}-pyridine-2-carboxylic acid methyl amide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(C)(C)OC(=O)n1cc(-c2cn(Cc3ccccc3)nn2)c2cccnc21
Reaction #73853
tert-butyl 3-(1-benzyl-1H-1,2,3-triazol-4-yl)pyrrolo[2,3-b]pyridine-1-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
Cn1cc(-c2cnc3c(c2)c(-c2cn(Cc4ccccc4)nn2)cn3C(=O)OC(C)(C)C)cn1
Reaction #73857
tert-butyl 3-(1-benzyl-1H-1,2,3-triazol-4-yl)-5-(1-methyl-1H-pyrazol-4-yl)pyrrolo[2,3-b]pyridine-1-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CCOC(=O)c1cn(Cc2ccccc2)nn1
Reaction #86836
ethyl 1-benzyl-1H-1,2,3-triazole-4-carboxylate
수율 24.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
c1ccc(Cn2cc(-c3ccccc3)nn2)cc1
Reaction #92775
1-benzyl-4-phenyl-1H-1,2,3-triazole
수율 95.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
c1ccc(Cn2cc(-c3ccccc3)nn2)cc1
Reaction #92776
1-benzyl-4-phenyl-1H-1,2,3-triazole
수율 95.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CCC[CH2][Sn]([CH2]CCC)([CH2]CCC)[c]1nnn(Cc2ccccc2)c1-c1ccccc1
Reaction #327943
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
CCC[CH2][Sn]([CH2]CCC)([CH2]CCC)[c]1nnn(Cc2ccccc2)c1C
Reaction #327946
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
N#Cc1cc(-c2nnn(Cc3ccccc3)c2I)ccc1F
Reaction #327947
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
CCC[CH2][Sn]([CH2]CCC)([CH2]CCC)[c]1nnn(Cc2ccccc2)c1CN1C(=O)c2ccccc2C1=O
Reaction #327948
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
CCC[CH2][Sn]([CH2]CCC)([CH2]CCC)[c]1nnn(Cc2ccccc2)c1C(=O)OC
Reaction #327950
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
CCC[CH2][Sn]([CH2]CCC)([CH2]CCC)[c]1nnn(Cc2ccccc2)c1-c1ccc(F)cc1
Reaction #327952
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
CCC[CH2][Sn]([CH2]CCC)([CH2]CCC)[c]1nnn(Cc2ccccc2)c1-c1ccccc1C
Reaction #327953
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
CCC[CH2][Sn]([CH2]CCC)([CH2]CCC)[c]1cn(Cc2ccccc2)nn1
Reaction #327979
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
Cc1cc(C2=NOC(c3cc(Cl)cc(Cl)c3)(C(F)(F)F)C2)sc1-c1cn(Cc2ccccc2)nn1
Reaction #329584
1-benzyl-4-{5-[5-(3,5-dichloro-phenyl)-5-trifluoromethyl-4,5-dihydro-isoxazol-3-yl]-3-methyl-thiophen-2-yl}-1H-[1,2,3]triazole
수율 25.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
Cc1cc(C)c(-c2nnn(Cc3ccccc3)c2N)c(C)c1
Reaction #364918
solid
수율 61.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_03
CCOC(=O)c1nnnn1Cc1ccccc1
Reaction #412921
ethyl 1-benzyl-1H-tetrazole-5-carboxylate
수율 93.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1984_04
Cc1cc(C)c(-c2nnn(Cc3ccccc3)c2N)c(C)c1
Reaction #456178
solid
수율 61.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_10
O=S(=O)(Cc1ccccc1)c1nnnn1Cc1ccccc1
Reaction #457711
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1985_07
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