N,N-diethylethanamine;hydrochloride

c1ccc(COc2ccc(-c3nnn[nH]3)cc2)cc1
Reaction #5040
5-(4-benzyloxyphenyl)tetrazole
Ausbeute 98.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
COC(=O)[C@@H](Cc1ccccc1)N=Cc1ccccc1
Reaction #6020
N-benzylidene-D-phenylalanine methyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
Clc1nn2c(-c3ccccc3)nnc2cc1C1CCC1
Reaction #11322
title compound
Ausbeute 34.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COc1cccc2c(Cl)nc(-c3ccccc3C(F)(F)F)nc12
Reaction #11918
solid
Ausbeute 89.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCCCCCCCOc1ccc(-c2nnn[nH]2)c(O)c1
Reaction #46735
5-Octyloxy-2-(1H-tetrazol-5-yl)-phenol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COc1cc(OCc2ccccc2)ccc1-c1nn[nH]n1
Reaction #51105
5-[4-(benzyloxy)2-methoxyphenyl]-2H-tetrazole
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CC(=O)O[C@@H]1C=Cc2ccccc2[C@H]1O
Reaction #57070
2
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
COc1cccc2c(Cl)nc(-c3ccccc3C(F)(F)F)nc12
Reaction #66458
solid
Ausbeute 89.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
COC(=O)[C@@H](C)Oc1ccc(C)cc1
Reaction #66576
(2R)-2-(4-methylphenoxy)-propanoic acid, methyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
C[C@H]1CN(c2ccc(C#N)cn2)CCN1
Reaction #70451
desired product
Ausbeute 69.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
C[C@@H]1CN(c2ccc(C#N)cn2)CCN1
Reaction #70452
desired product
Ausbeute 59.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CCCCC/C=C\C/C=C\C/C=C\C/C=C\CCCC(=O)NCCSSCCNC(=O)CCC/C=C\C/C=C\C/C=C\C/C=C\CCCCC
Reaction #75531
N,N′-diarachidonoylcystamine
Ausbeute 75.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
Clc1ccc(Nc2nnc(Cc3ccncc3)c3ccccc23)cc1
Reaction #78138
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
Fc1ccc(Nc2nnc(Cc3ccncc3)c3ccccc23)cc1Cl
Reaction #78162
Title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
Cc1cccc(Nc2nnc(Cc3ccncc3)c3ccccc23)c1
Reaction #78163
Title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
CC(C)(C)c1ccc(Nc2nnc(Cc3ccncc3)c3ccccc23)cc1.Cl.Cl
Reaction #78164
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
c1ccc(-c2ccc(Nc3nnc(Cc4ccncc4)c4ccccc34)cc2)cc1
Reaction #78169
Title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
Cc1cc(Cc2nnc(Nc3ccc(Cl)cc3)c3ccccc23)ccn1
Reaction #78174
Title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
CC(c1ccncc1)c1nnc(Nc2ccc(Cl)cc2)c2ccccc12
Reaction #78177
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
CC(C)(C)OC(=O)N1CCC(N(CCc2ccc(Cl)cc2)Cc2cccc(-c3nnn[nH]3)c2)CC1
Reaction #88072
tert-Butyl 4-((3-(1H-tetrazol-5-yl)benzyl)(4-chlorophenethyl)amino)piperidine-1-carboxylate
Ausbeute 60.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
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