2-methoxyethylamine

COCCNC(=O)COc1ccc(C(=O)CN2CCN(c3ccncc3)CC2)cc1
Reaction #2318
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCCc1nc(C)n2c(=O)[nH]c(-c3cc(S(=O)(=O)NCCOC)ccc3OCC)nc12
Reaction #8723
4-Ethoxy-N-(2-methoxy-ethyl)-3-(6-methyl-4-oxo-8-propyl-3,4-dihydro-imidazo[1,5-a][1,3,5]triazin-2-yl)-benzenesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COCCNc1ccc(C(=O)c2sc(Nc3ccc(N4CCN(C)CC4)cc3)nc2N)cc1[N+](=O)[O-]
Reaction #10902
[4-Amino-2-[[4-(4-methyl-1-piperazinyl)phenyl]amino]-5-thiazolyl][3-nitro-4-[(2-methoxyethyl)amino]phenyl]methanone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCOC(=O)c1cn(-c2ccc3c(c2)CCC3)c2nc(NCCOC)ncc2c1=O
Reaction #40620
8-indan-5-yl-2-(2-methoxy-ethylamino)-5-oxo-5,8-dihydro-pyrido[2,3-d]pyrimidine-6-carboxylic acid ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
—
Reaction #40637
solid
Ausbeute 80.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COCCNc1c(C(=O)NC2C3CC4CC(C3)CC2C4)cnn1C
Reaction #41124
5-(2-Methoxy-ethylamino)-1-methyl-1H-pyrazole-4-carboxylic acid adamantan-2-ylamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COCCNC(=O)c1cnc(CNC(=O)OC(C)(C)C)c2c(OC)cc(OC)cc12
Reaction #42909
[6,8-dimethoxy-4-(2-methoxy-ethylcarbamoyl)-isoquinolin-1-ylmethyl]carbamic acid tert-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COCCNC(=O)c1cnc(CNC(=O)OC(C)(C)C)c2cc(OC)c(OC)cc12
Reaction #42933
[6,7-dimethoxy-4-(2-methoxy-ethylcarbamoyl)-isoquinolin-1-ylmethyl]-carbamic acid tert-butyl ester
Ausbeute 49.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COCCNC(=O)Cc1cnc(CNC(=O)OC(C)(C)C)c2cc(OC)c(OC)cc12
Reaction #42956
{6,7-dimethoxy-4-[(2-methoxy-ethylcarbamoyl)-methyl]-isoquinolin-1-ylmethyl}-carbamic acid tert-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COCCNCc1cc(Br)cnc1N
Reaction #46585
title compound
Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COCCNCc1ccc2c(c1)cc(-c1ccc(Cl)c3c1C(=O)NC3)n2C(=O)OC(C)(C)C
Reaction #49326
4-chloro-7-[1-(tert-butoxycarbonyl)-5-[(2-methoxyethyl)aminomethyl]indol-2-yl]isoindolinone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COCCNCc1ccc2c(c1)cc(-c1cc(OC)c(OS(C)(=O)=O)c3c1C(=O)NC3)n2C(=O)OC(C)(C)C
Reaction #49564
4-methanesulfonyloxy-5-methoxy-7-[1-(tert-butoxycarbonyl)-5-(2-methoxyethylaminomethyl)indol-2-yl]isoindolinone
Ausbeute 56.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COCCNCc1cccc2c1cc(-c1cc(OC)c(OS(C)(=O)=O)c3c1C(=O)NC3)n2C(=O)OC(C)(C)C
Reaction #49585
4-methanesulfonyloxy-5-methoxy-7-[1-(tert-butoxycarbonyl)-4-(2-methoxyethylaminomethyl)indol-2-yl]isoindolinone
Ausbeute 34.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COCCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1cnc2n1[C@](C)(Cc1ccc(-c3cncnc3)cc1)C(=O)N2c1cc(Cl)cc(Cl)c1
Reaction #52119
title compound
Ausbeute 44.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
COCCNS(=O)(=O)c1ccc(N)cc1
Reaction #52200
title compound
Ausbeute 65.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
COCCNS(=O)(=O)c1ccc(Cl)cc1Cl
Reaction #52202
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
COCCNCc1c(C(=O)c2ccc(Cl)cc2Cl)oc2cc(Br)ccc12
Reaction #57521
desired product
Ausbeute 48.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
COCCNC(=O)c1cccc(-c2ccc3c(C)c(C(=O)c4ccc(Cl)cc4Cl)oc3c2)c1
Reaction #57528
desired product
Ausbeute 25.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
COCCNCc1cccc(Br)n1
Reaction #58756
title compound
Ausbeute 94.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
COCCNS(=O)(=O)c1ccc(Nc2nccc(-c3cnc(C=O)n3C(C)C)n2)cc1
Reaction #60626
title compound
Ausbeute 24.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
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