2-ethoxyethanol

Nc1ncc2cc(-c3c(Cl)cccc3Cl)c(N)nc2n1
Reaction #3259
2,7-diamino-6-(2,6-dichlorophenyl)-pyrido[2,3-d]-pyrimidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCn1c(=N)c(-c2ccsc2)cc2cnc(Nc3ccccc3)nc21
Reaction #3320
(8-ethyl-7-imino-6-thiophen-3-yl-7,8-dihydro-pyrido[2,3-d]pyrimidin-2-yl)-phenylamine
Выход 78.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCn1c(=N)c(-c2cccs2)cc2cnc(Nc3ccccc3)nc21
Reaction #3321
(8-ethyl-7-imino-6-thiophen-2-yl-7,8-dihydro-pyrido[2,3-d]pyrimidin-2-yl)-phenylamine
Выход 85.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCn1c(=N)c(-c2ccc3ccccc3c2)cc2cnc(Nc3ccccc3)nc21
Reaction #3330
yellow solid
Выход 82.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(O)Cc1ccc(-n2sc3ccccc3c2=O)cc1
Reaction #3366
title compound
Выход 69.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Nc1ncc2cc(-c3c(Cl)cccc3Cl)c(N)nc2n1
Reaction #3504
2,7-diamino-6-(2,6-dichlorophenyl)-pyrido[2,3-d]pyrimidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Nc1ncc2cc(-c3c(Br)cccc3Br)c(N)nc2n1
Reaction #3540
6-(2,6-dibromo-phenyl)-pyrido[2,3-d]pyrimidine-2,7-diamine
Выход 63.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Nc1nc2nc(Nc3ccccc3)ncc2cc1-c1c(Cl)cccc1Cl
Reaction #3543
title compound
Выход 68.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Nc1ncc2cc(-c3ccncc3)c(N)nc2n1
Reaction #3576
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1cccc(-c2noc3ccsc23)c1
Reaction #8738
title compound
Выход 68.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CN(CCCNC(=O)OC(C)(C)C)CCCNc1c2nc3ccccc3c-2n(C)c2ccccc12
Reaction #40538
[3-[methyl-[3-(5-methyl-5H-indolo[3,2-b]quinolin-11-yl-amino)propyl]-amino]propyl]carbamic acid tert-butyl ester
Выход 490.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
NC(=O)c1sc2c(ccc(=O)n2-c2ccsc2)c1Nc1ccccc1
Reaction #58707
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
N#Cc1ccccc1Nc1c(C(N)=O)sc2c1ccc(=O)n2-c1ccsc1
Reaction #58708
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
COCc1nc(CO)c(Cl)n1C
Reaction #78657
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
COc1cc(CN=C2C=Cc3nc(N)nc(N)c3C2)cc(OC)c1OC
Reaction #80895
2,4-diamino-6-[(3,4,5-trimethoxyphenylmethyl)imino]quinazoline
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
Cc1c([N+](=O)[O-])ccc2nc(N)nc(N)c12
Reaction #80912
2,4-diamino-5-methyl-6-nitroquinazoline
Выход 82.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
Nc1ncc2cc(-c3c(Cl)cccc3Cl)c(N)nc2n1
Reaction #81899
2,7-diamino-6-(2,6-dichlorophenyl)-pyrido[2,3-d]-pyrimidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
O=C(O)Cc1ccc(-n2sc3ccccc3c2=O)cc1
Reaction #81960
title compound
Выход 69.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
Cn1c2cc(Br)sc2c2cn[nH]c(=O)c21
Reaction #164618
pyridazinone
Выход 94.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Nc1cccc(Nc2nccc(Sc3ccccc3)n2)c1
Reaction #168890
product
Выход 42.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
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