N,N′-dimethylethane-1,2-diamine

CC(=O)c1ccc(-c2ccccc2)c(-c2ccccc2)n1
Reaction #40831
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCC(=O)c1ccc(-c2ccccc2)c(-c2ccccc2)n1
Reaction #40832
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(=O)c1ccc(-c2ccc(C(F)(F)F)cc2)c(-c2ccccc2)n1
Reaction #40833
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCC(=O)c1ccc(-c2ccc(C(F)(F)F)cc2)c(-c2ccccc2)n1
Reaction #40834
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCC(=O)c1ccc(-c2ccccc2)c(-c2ccc(C(F)(F)F)cc2)n1
Reaction #40835
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(=O)c1cnc(-c2ccccc2)c(-c2ccccc2)n1
Reaction #40845
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCC(=O)c1cnc(-c2ccccc2)c(-c2ccccc2)n1
Reaction #40846
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=C1OCCN1c1cccc(CCO)c1
Reaction #44135
title compound
Выход 64.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CNCCN(C)Cc1ccc(C(=O)OC)cc1
Reaction #44762
methyl 4-[(methyl(2-(methylamino)ethyl)amino)methyl]benzoate
Выход 62.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCOC(=O)c1c(C)n(-c2ccccc2)c2ccc(OCc3ccccc3)cc12
Reaction #44911
5-benzyloxy-2-methyl-1-phenyl-1H-indole-3-carboxylic acid, ethyl ester
Выход 76.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC1(C)c2cc(Br)ccc2-c2ccc(N(c3ccccc3)c3ccccc3)cc21
Reaction #60235
yellow solid
Выход 69.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
Brc1ccc(N(c2ccccc2)c2ccccc2)cc1
Reaction #60236
white crystal
Выход 70.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
Cn1cnc(-c2cccc(NC(=O)OC(C)(C)C)c2)c1-c1cc2c(N)ncnc2s1
Reaction #60911
title compound
Выход 9.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CN1CCN(C)C(=O)C1
Reaction #64008
1,4-dimethylpiperazin-2-one
Выход 93.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
Cn1cc(C(=O)Nc2cccc3c2C2CCC3C2=C(Cl)Cl)c(C(F)F)n1
Reaction #67692
3-difluoromethyl-1-methyl-1H-pyrazole-4-carboxylic acid (9-dichloromethylene-1,2,3,4-tetrahydro-1,4-methano-naphthalen-5-yl)-amide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
—
Reaction #69108
solid
Выход 60.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
COc1cc(S(C)(=O)=O)ccc1O
Reaction #70430
title compound
Выход 52.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
O=C1CCCN1c1ccc(Cl)nc1
Reaction #70458
desired product
Выход 103.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
Cc1cn(C(C)C)c2cc(S(C)(=O)=O)cc(C(=O)O)c12
Reaction #70793
title compound
Выход 25.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CC(C)n1ccc2c(C(=O)O)cc(S(C)(=O)=O)cc21
Reaction #70794
product
Выход 9.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
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