ethanamine

CCNC=C(C(=O)OCC)C(=O)c1c(F)cc(F)c(F)c1C
Reaction #1378
ethyl 2-(2-methyl-3,4,6-trifluorobenzoyl)-3-ethylaminoacrylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCNCc1ccc(-c2ccccc2CNC(=O)OC(C)(C)C)cc1
Reaction #2017
desired product
Rendimiento 68.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCNc1ncc2cc(-c3c(Cl)cccc3Cl)c(=O)n(C)c2n1
Reaction #3280
6-(2,6-Dichlorophenyl)-2-ethylamino-8-methyl-8H-pyrido[2,3-d]pyrimidin-7-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCNc1nc(SC)ncc1C(=O)OCC
Reaction #3315
4-ethylamino-2-methylthio-5-pyrimidinecarboxylate ethyl ester
Rendimiento 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCNC(=O)[C@@H]1C[C@H](O)CN1C(=O)OC(C)(C)C
Reaction #5194
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CCNc1nc2ccc([N+](=O)[O-])cc2cc1C
Reaction #6901
N-ethyl-3-methyl-6-nitroquinolin-2-amine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCNC(=O)c1ccc(CN([C@H]2CCCCC[C@H]2C(N)=O)S(=O)(=O)c2ccc(Cl)cc2)cc1
Reaction #7144
titled compound
Rendimiento 18.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCNc1cc(OCCCN(CC)CC)ccc1[N+](=O)[O-]
Reaction #8149
2-(ethylamino)-4-(3-diethylamino-1-propoxy)nitrobenzene
Rendimiento 88.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCNC(=O)CC[C@H](N)C(=O)O
Reaction #10462
L-theanine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCNC(=O)[C@H]1O[C@@H](OC)[C@@H]2OC(C)(C)O[C@@H]21
Reaction #10539
title compound
Rendimiento 94.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCNC(=O)[C@H]1O[C@@H](n2cnc3c(NCC(c4ccccc4)c4ccccc4)nc(C(=O)OCC)nc32)[C@@H]2OC(C)(C)O[C@@H]21
Reaction #10566
title compound
Rendimiento 78.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCNCc1cccc(-c2ccnc(Cl)n2)c1
Reaction #43053
[3-(2-chloro-pyrimidin-4-yl)-benzyl]-ethyl-amine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCNCc1cccc(-c2ccnc(NCCc3ccc(O)cc3)n2)c1
Reaction #43122
4-{2-[4-(3-Ethylaminomethyl-phenyl)-pyrimidin-2-ylamino]-ethyl}-phenol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCNC(=O)C1CCC(CC#Cc2nc(N)c3ncn(C4OC(C(=O)NCC)C(O)C4O)c3n2)CC1
Reaction #44341
JR3037
Rendimiento 73.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCNC1C(C(=O)OCC)=C(c2ccccc2)c2ccc(OC)cc21
Reaction #47841
titled compound
Rendimiento 75.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCNCc1ccc2c(c1)cc(-c1ccc(Cl)c3c1C(=O)NC3)n2C(=O)OC(C)(C)C
Reaction #49306
4-chloro-7-[1-(tert-butoxycarbonyl)-5-(ethylaminomethyl)indol-2-yl]isoindolinone
Rendimiento 83.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCNCCS(=O)(=O)Oc1ccc(-c2cc3cc(CN4CCCCC4)ccc3n2C(=O)OC(C)(C)C)c2c1CNC2=O
Reaction #49410
4-[2-(ethylamino)ethanesulfonyloxy]-7-[1-(tert-butoxycarbonyl)-5-(piperidinomethyl)indol-2-yl]isoindolinone
Rendimiento 43.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCN=C(CCNC(=O)c1cc([N+](=O)[O-])cn1CCC(C)C)NCC
Reaction #51435
Compound 272
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CCNC(=O)c1ccc(C(c2ccc(Cl)cc2)N2CC(=C(c3cc(F)cc(F)c3)S(C)(=O)=O)C2)cc1
Reaction #53460
(RS)-1-{(4-chlorophenyl)[4-(N-ethylcarbamoyl)phenyl]methyl}-3-[(3,5-difluorophenyl)(methylsulfonyl)methylene]azetidine
Rendimiento 29.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CCNCC(O)c1ccc2c(c1)OCO2.Cl
Reaction #54280
1-(3,4-methylenedioxyphenyl)-2-ethylaminoethanol hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_04
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