dichloromethane;ethoxyethane

C=CCN1CCCN(c2ccc(C(=O)Nc3cc(CCc4cc(OC)cc(OC)c4)n[nH]3)cc2)CC1
Reaction #45160
title compound
Rendimiento 14.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COc1cc(CCc2cc(NC(=O)c3ccc(N4CCCN(C5CC5)CC4)cc3)[nH]n2)cc(OC)c1
Reaction #45163
title compound
Rendimiento 33.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COc1cc(CCc2cc(NC(=O)c3ccc(N4CCCN(C(C)C)CC4)cc3)[nH]n2)cc(OC)c1
Reaction #45165
title compound
Rendimiento 42.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCN1CCCN(c2ccc(C(=O)Nc3cc(CCc4cc(OC)cc(OC)c4)n[nH]3)cc2)CC1
Reaction #45172
title compound
Rendimiento 25.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCCN1C(=O)C2(c3ccc(N)cc3)CC(c3ccc(N)cc3)(C2)C1=O
Reaction #63362
1,5-di-(4-aminophenyl)-3-n-propyl-3-azabicyclo[3.1.1]heptane-2,4-dione
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
N#Cc1cccc(C2C=C(C(F)(F)F)NC3=C2C(=O)CCC3)c1
Reaction #82739
title compound
Rendimiento 99.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
CNc1ccccc1C(=O)OCCCC1CCC(=O)CC1=O
Reaction #164454
6
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CN[C@@H]1CCN(c2ccnc(Cl)c2)C1
Reaction #164483
desired product
Rendimiento 100.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CN1C(=O)Cc2cccc(C(=O)c3ccccc3)c21
Reaction #323550
1-methyl-7-benzoyloxindole
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1987_02
CC(C)NCCCS(=O)(=O)O
Reaction #326889
powder
Rendimiento 65.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
Cl.Cl.NCC1(c2ccc(OCCCN3CCCC3)cc2)CCOCC1
Reaction #360040
title compound
Rendimiento 81.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_11
CCCCCCCCCC(=O)C=CC(=O)O
Reaction #361127
4-ketotridec-2-enoic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_02
CCCC(=O)C=CC(=O)O
Reaction #361128
4-keto-hept-2-enoic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_02
CCCCCc1c(C(C)C)nc(C(C)C)c(CN(C)C)c1-c1ccc(F)cc1
Reaction #412017
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_04
CCCCCc1c(C(C)C)nc(C(C)C)c(CNCC)c1-c1ccc(F)cc1
Reaction #412018
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_04
CCOC(=O)Cc1cc(C)c(C(=O)OCC)n1C
Reaction #412596
ethyl-1,4 dimethyl-5-ethoxycarbonylpyrrole-2-acetate
Rendimiento 87.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1984_04
CCCCCCCCCC(=O)C=CC(=O)O
Reaction #413535
4-ketotridec-2-enoic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_12
CCCC(=O)C=CC(=O)O
Reaction #413536
4-keto-hept-2-enoic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_12
COC(=O)c1ccccc1CC(=O)Nc1cccc(/C=C/c2nc(C3CCC3)cs2)c1
Reaction #414724
(E)-2-[2-[3-[2-[4-(cyclobutyl)-2-thiazolyl]ethenyl]phenylamino]-2-oxoethyl]benzoic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_12
CCN(CCO)CCC[C@@H](Oc1cc(Cl)ccc1C#N)c1ccccc1.Cl
Reaction #439289
title compound
Rendimiento 65.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_06
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