DCM water

C=C1CN(C(=O)Cc2ccc(F)cc2)N(C(=O)OCc2ccccc2)C1
Reaction #7738
desired product
Ausbeute 62.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCOC(=O)/C=C/c1ccc(CBr)cc1C
Reaction #9728
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CN1CCC(c2cccc3c2cc(C(N)=O)n3Cc2cccc(F)c2)CC1
Reaction #46443
1-(3-Fluoro-benzyl)-4-(1-methyl-piperidin-4-yl)-1H-indole-2-carboxylic acid amide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
C=C1CN(C(=O)Cc2ccc(F)cc2)N(C(=O)OCc2ccccc2)C1
Reaction #50946
desired product
Ausbeute 62.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CC(C)(C)[Si](C)(C)O[C@H](CCO)CCc1ccccc1
Reaction #52061
(S)-3-(t-butyldimethylsilyloxy)-5-phenyl-pentan-1-ol
Ausbeute 99.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
Brc1ccn(C(c2ccccc2)(c2ccccc2)c2ccccc2)n1
Reaction #61070
title compound
Ausbeute 64.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
Cc1[nH]c2ccc(Cl)cc2c1SC1CCN(CCn2cccc2)CC1
Reaction #65165
5-chloro-2-methyl-3-[[1-[2-(1H-pyrrol-1-yl)ethyl]piperidin-4-yl]thio]-1H-indole
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
COc1cc(OC)c(Cl)c(-c2ccc(C(=O)Nc3nc(CN(C)CCN(C)C)c[nH]3)c3nccnc23)c1Cl
Reaction #71498
title compound
Ausbeute 59.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
COC(=O)c1cc(F)nc2ccccc12
Reaction #75705
2-fluoroquinoline-4-carboxylic acid methyl ester
Ausbeute 66.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
COc1ccc(OC2CCCCO2)cn1
Reaction #85028
2-Methoxy-5-(tetrahydro-2H-pyran-2-yloxy)pyridine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
BrCc1cc(I)cc(I)c1I
Reaction #86633
2,3,5-triiodobenzyl bromide
Ausbeute 85.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
COCCOc1ccn2c(C(=O)Nc3cccc4c3c(OC)nn4Cc3ccc(C)nc3)cnc2c1
Reaction #166650
N-(3-methoxy-1-((6-methylpyridin-3-yl)methyl)-1H-indazol-4-yl)-7-(2-methoxyethoxy)imidazo[1,2-a]pyridine-3-carboxamide
Ausbeute 49.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC1C(=O)Nc2ccccc2-c2ccccc21
Reaction #220422
title compound
Ausbeute 63.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
C/C(=C\[C@H](C(C)C)N(C)C(=O)[C@@H](NC(=O)[C@@H]1CCCN1C)C(C)(C)C)C(=O)O
Reaction #220996
product
Ausbeute 28.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
CCOCn1ccnc1C(=O)C(C)=CC(CC(=O)C(NC(=O)OC(C)(C)C)C(C)(C)C)C(C)C
Reaction #221013
(1-{[4-(-Ethoxymethyl-1H-imidazol-2-yl)-1-isopropyl-3-methyl-4-oxo-but-2-enyl]-methyl-carbonyl}-2,2-dimethyl-propyl)-carbamic acid tert-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
CCOC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)OC(C)(C)C
Reaction #340917
N-(tert-butoxycarbonyl)-L-tyrosine ethyl ester
Ausbeute 180.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_01
C#CCOC(=O)Oc1ccc(Cc2ccc(OC(=O)OCC#C)cc2)cc1
Reaction #343931
title compound
Ausbeute 93.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_11
C#CCOC(=O)Oc1ccc(-c2ccc(OC(=O)OCC#C)cc2)cc1
Reaction #343932
title compound
Ausbeute 93.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_11
CCOC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)OC(C)(C)C
Reaction #360446
N-(tert-butoxycarbonyl)-L-tyrosine ethyl ester
Ausbeute 180.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_11
N#Cc1ccc2cc(C(=O)O)ccc2c1
Reaction #412245
desired compound
Ausbeute 86.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_04
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