fumaric acid

CN1CCCC1c1cncc(-c2ccc(Cl)cc2)c1.O=C(O)/C=C/C(=O)O
Reaction #1127
5-(4-chlorophenyl)-3-(1-methyl-2-pyrrolidinyl)pyridine fumarate
Выход 72.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CN1CCCC1c1cncc(-c2ccc(F)cc2)c1.O=C(O)/C=C/C(=O)O
Reaction #1128
5-(4-fluorophenyl)-3-(1-methyl-2-pyrrolidinyl)pyridine fumarate
Выход 63.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CN1CCCC1c1cncc(-c2ccco2)c1.O=C(O)/C=C/C(=O)O
Reaction #1129
5-(2-furanyl)-3-(1-methyl-2-pyrrolidinyl)pyridine fumarate
Выход 43.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CN1CCCC1c1cncc([Si](C)(C)C)c1.O=C(O)/C=C/C(=O)O
Reaction #1130
5-trimethylsilyl-3-(1-methyl-2-pyrrolidinyl)pyridine fumarate
Выход 51.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CN1CCCC1c1cncc(C#Cc2ccccc2)c1.O=C(O)/C=C/C(=O)O
Reaction #1131
5-(phenylethynyl)-3-(1-methyl-2-pyrrolidinyl)pyridine fumarate
Выход 56.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Fc1ccc(-c2cncc(C3CCCCN3)c2)cc1.O=C(O)/C=C/C(=O)O
Reaction #1136
5-(4-fluorophenyl)-3-(2-piperidinyl)pyridine fumarate
Выход 70.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1cccc(N(CCN2CCC(C(=O)c3ccc(F)cc3)CC2)C(=O)c2ccc(NC(C)=O)cc2)c1.O=C(O)/C=C/C(=O)O
Reaction #2620
title compound
Выход 80.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1cccc(N(CCN2CCC(C(=O)c3ccc(F)cc3)CC2)C(=O)c2ccc(N)cc2)c1.COc1cccc(N(CCN2CCC(C(=O)c3ccc(F)cc3)CC2)C(=O)c2ccc(N)cc2)c1.O=C(O)/C=C/C(=O)O
Reaction #2624
title compound
Выход 90.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(O)/C=C/C(=O)O.O=CNc1ccc(C(=O)N(CCN2CCC(C(=O)c3ccc(F)cc3)CC2)c2cccnc2)cc1.O=CNc1ccc(C(=O)N(CCN2CCC(C(=O)c3ccc(F)cc3)CC2)c2cccnc2)cc1
Reaction #2625
title compound
Выход 52.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCCCC(=O)Nc1ccc(C(=O)N(CCN2CCC(C(=O)c3ccc(F)cc3)CC2)c2cccnc2)cc1.CCCCC(=O)Nc1ccc(C(=O)N(CCN2CCC(C(=O)c3ccc(F)cc3)CC2)c2cccnc2)cc1.O=C(O)/C=C/C(=O)O
Reaction #2626
title compound
Выход 84.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CNc1ccc(C(=O)N(CCN2CCC(C(=O)c3ccc(F)cc3)CC2)c2cccnc2)cc1.CNc1ccc(C(=O)N(CCN2CCC(C(=O)c3ccc(F)cc3)CC2)c2cccnc2)cc1.O=C(O)/C=C/C(=O)O
Reaction #2627
title compound
Выход 79.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CS(=O)(=O)Nc1ccc(C(=O)N(CCN2CCC(C(=O)c3ccc(F)cc3)CC2)c2cccnc2)cc1.CS(=O)(=O)Nc1ccc(C(=O)N(CCN2CCC(C(=O)c3ccc(F)cc3)CC2)c2cccnc2)cc1.O=C(O)/C=C/C(=O)O
Reaction #2628
title compound
Выход 43.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCOC(=O)Nc1ccc(C(=O)N(CCN2CCC(C(=O)c3ccc(F)cc3)CC2)c2cccnc2)cc1.CCOC(=O)Nc1ccc(C(=O)N(CCN2CCC(C(=O)c3ccc(F)cc3)CC2)c2cccnc2)cc1.O=C(O)/C=C/C(=O)O
Reaction #2629
title compound
Выход 75.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
NC(=O)Nc1ccc(C(=O)N(CCN2CCC(C(=O)c3ccc(F)cc3)CC2)c2cccnc2)cc1.NC(=O)Nc1ccc(C(=O)N(CCN2CCC(C(=O)c3ccc(F)cc3)CC2)c2cccnc2)cc1.O=C(O)/C=C/C(=O)O
Reaction #2630
title compound
Выход 56.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CN(C)CCC1CN(C)C(=S)c2cccnc2O1.O=C(O)/C=C/C(=O)O
Reaction #4924
2-[2-(Dimethylamino)ethyl]-2,3-dihydro-4-methylpyrido[3,2-f][1,4]-oxazepine-5(4H)-thione fumarate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
CN1CC(CCN2CCCC2)Oc2ncccc2C1=O.O=C(O)/C=C/C(=O)O
Reaction #4932
2,3-Dihydro-4-methyl-2-[2-(1-pyrrolidinyl)ethyl]pyrido[3,2-f][1,4]-oxazepin-5(4H)-one fumarate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
CC(C)O.CC1CCCN1CCC1CN(C)C(=S)c2cccnc2O1.O=C(O)/C=C/C(=O)O
Reaction #4947
yellow crystals
Выход 32.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
Cc1ccc2c(n1)OC(CCN(C)C)CN(C)C2=O.O=C(O)/C=C/C(=O)O
Reaction #4962
2-[2-(Dimethylamino)ethyl]-2,3-dihydro-4,8-dimethylpyrido[3,2-f][1,4]-oxazepin-5(4H)-one fumarate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
CCOC(=O)C1=C(CSCCN)NC(C)=C(C(=O)OC)C1c1cccc([N+](=O)[O-])c1.O=C(O)/C=C/C(=O)O
Reaction #5745
(-)-2-(aminoethylthio)methyl-3-carboethoxy-5-carbomethoxy-4-(3-nitrophenyl)-6-methyl-1,4-dihydropyridine fumarate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CC(C)N1CCN(C(=O)c2ccc(CN3CCOCC3)cc2)CC1.O=C(O)/C=C/C(=O)O
Reaction #41817
crude title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
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