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651446

CCOC(=O)c1cnc(N[C@@H]2C[C@H]3CC[C@@H]2C3)nc1C(C)C
Reaction #67039
ethyl rac-2-[(1R,2R,4S)-bicyclo[2.2.1]hept-2-ylamino]-4-isopropylpyrimidine-5-carboxylate
Ausbeute 84.4%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cnc(N[C@H]2C[C@@H]3CC[C@H]2C3)nc1C(C)C
Reaction #67040
ethyl 2-[(1S,2S,4R)-bicyclo[2.2.1]hept-2-ylamino]-4-isopropylpyrimidine-5-carboxylate
Ausbeute 93.6%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cnc(Nc2ccc(OC(F)F)cc2)nc1OC
Reaction #164645
ethyl 2-((4-(difluoromethoxy)phenyl)amino)-4-methoxypyrimidine-5-carboxylate
Ausbeute 71.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cnc(N2CCC(N)C2)nc1
Reaction #179623
DOI: 10.1039/C8SC04228D
CCCCN(C)c1ncc(C(=O)OCCC(C)=C(F)F)c(C)n1
Reaction #185249
DOI: 10.1039/C8SC04228D
CCOC(=O)c1cnc(NCCCC2CCN(C)CC2)nc1C
Reaction #236122
DOI: 10.1039/C8SC04228D
CC(CCOC(=O)c1cnc(OCCCCCl)nc1C)=C(F)F
Reaction #247185
DOI: 10.1039/C8SC04228D
CCOC(=O)c1cnc(Oc2ccc(F)cc2F)nc1NN
Reaction #316583
2-(2,4-difluoro-phenoxy)-4-hydrazino-pyrimidine-5-carboxylic acid ethyl ester
Ausbeute 53.3%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cnc(N2CCN(S(=O)(=O)c3ccc4ccccc4c3)CC2)nc1
Reaction #507619
2-[4-(2-naphthalenylsulfonyl)-1-piperazinyl]- 5-pyrimidinecarboxylic acid, ethyl ester
Ausbeute 84.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1c(C)nc(N[C@@H]2CCCC[C@@H]2NC(=O)OC(C)(C)C)nc1-c1cnn(C)c1C
Reaction #603213
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cnc(N2CCN(S(=O)(=O)c3ccc4ccccc4c3)CC2)nc1
Reaction #625267
2-[4-(2-naphthalenylsulfonyl)-1-piperazinyl]-5-pyrimidinecarboxylic acid, ethyl ester
Ausbeute 84.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cnc(N2CCN(S(=O)(=O)c3ccc4ccccc4c3)CC2)nc1
Reaction #732606
2-[4-(2-naphthalenylsulfonyl)-1-piperazinyl]-5-pyrimidinecarboxylic acid, ethyl ester
Ausbeute 84.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CCOC(=O)c1c(Cl)nc(C#N)nc1OCCC1CCN(C(=O)OC(C)(C)C)CC1
Reaction #732697
4-[2-(1-tert-butoxycarbonylpiperidin-4-yl)ethoxy]-6-chloro-2-cyanopyrimidine-5-carboxylic acid allyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cnc(N2CCN(C3=Nc4ccccc4Oc4ccc(Cl)cc43)CC2)nc1
Reaction #769147
DOI: 10.1039/C8SC04228D
CCOC(=O)c1c(C)nc(N[C@@H]2CCCC[C@@H]2NC(=O)OC(C)(C)C)nc1-c1cnn(C)c1C
Reaction #798676
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cnc(N2CCN(C3=Nc4ccccc4Oc4ccc(Cl)cc43)CC2)nc1
Reaction #805240
title compound 116
Ausbeute 100.2%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cnc(N2C[C@@H]3C[C@H]2CN3C(c2ccccc2)c2ccccc2)nc1
Reaction #805245
title compound 202
Ausbeute 64.3%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cnc(OCc2ccccn2)nc1NCc1ccc(OC)c(Cl)c1
Reaction #923724
DOI: 10.1039/C8SC04228D
CC(CCOC(=O)c1cnc(S(C)(=O)=O)nc1C)=C(F)F
Reaction #1004559
4,4-difluoro-3-methyl-3-butenyl 2-methanesulfonyl-4-methylpyrimidine-5-carboxylate
Ausbeute 92.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCN(C)c1ncc(C(=O)OCCC(C)=C(F)F)c(C)n1
Reaction #1004560
4,4-difluoro-3-methyl-3-butenyl 2-(N-butyl-N-methylamino)-4-methylpyrimidine-5-carboxylate
Ausbeute 80.0%DOI: 10.6084/m9.figshare.5104873.v1
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