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818159

O=C(NCCCCc1ccccc1OCC(O)CO)OCc1ccccc1
Reaction #53397
Compound 31
Ausbeute 62.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCN(c2cccc(-n3ncc4cnc(-c5cncc(C(O)CO)n5)cc43)n2)CC1
Reaction #86275
tert-butyl 4-(6-(6-(6-(1,2-dihydroxyethyl)pyrazin-2-yl)-1H-pyrazolo[4,3-c]pyridin-1-yl)pyridin-2-yl)piperazine-1-carboxylate
Ausbeute 67.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NC1=N[C@@]2(c3cc(Br)ccc3F)CO[C@@H](C(=O)O)C[C@H]2CS1)c1ccccc1
Reaction #155598
product
Ausbeute 113.7%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCCCCc1ccccc1OCC(O)CO)OCc1ccccc1
Reaction #168480
Compound 31
Ausbeute 62.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCCCCc1ccccc1OCC(O)CO)OCc1ccccc1
Reaction #305089
Compound 31
Ausbeute 62.0%DOI: 10.6084/m9.figshare.5104873.v1
OCC(O)Cn1ncc2c1CCc1c-2sc2ncnc(Nc3ccc(OCc4cccc(F)c4)c(Cl)c3)c12
Reaction #309226
3-[6-({3-chloro-4-[(3-fluorobenzyl)oxy]phenyl}amino)-4,5-dihydro-3H pyrimido[5′,4′:4,5]thieno[2,3-e]indazol-3-yl]propane-1,2-diol
Ausbeute 8.9%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)Nc1nc(Nc2ccc(CN3CCOCC3)cc2)ncc1C(N)=O
Reaction #357028
2-{[4-(morpholinomethyl)phenyl]amino}-4-(2-propylamino)pyrimidine-5-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)c1cnc(Nc2ccc(CN3CCOCC3)cc2)nc1NC1CC1
Reaction #357029
4-cyclopropylamino-2-(4-morpholin -4-ylmethylphenylamino)-pyrimidine-5-carboxamide
Ausbeute 23.6%DOI: 10.6084/m9.figshare.5104873.v1
C=CCN1CC2CC(C1)c1cccc(C=O)c1C2=O
Reaction #359788
oil
Ausbeute 81.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C(=O)N1CC(O)C(O)C1)S(=O)(=O)CC(Cc1ccccc1)C(=O)OCc1ccccc1
Reaction #362781
benzyl (RS)-α-[[[1-[[(3RS,4RS)-3,4-dihydroxy-1-pyrrolidinyl]carbonyl]-1-methylethyl]sulfonyl]methyl]hydrocinnamate
Ausbeute 74.7%DOI: 10.6084/m9.figshare.5104873.v1
O=C1C(c2cccnc2)=C(c2ccccc2)c2ccc(OCC[N+]3([O-])CCOCC3)cc21
Reaction #418473
title compound
Ausbeute 26.8%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #507948
liquid
Ausbeute 48.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCCCCc1ccccc1OCC(O)CO)OCc1ccccc1
Reaction #544404
Compound 31
Ausbeute 62.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCCCCc1ccccc1OCC(O)CO)OCc1ccccc1
Reaction #544767
Compound 31
Ausbeute 62.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCCCCc1ccccc1OCC(O)CO)OCc1ccccc1
Reaction #545841
Compound 31
Ausbeute 62.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(O)(CO)c1nc(Br)ccc1F
Reaction #561242
solid
Ausbeute 91.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc2c(c3[nH]c4cc5ccccc5cc4c(=O)c13)C(=O)C(O)C(C)(C)O2
Reaction #565877
2-Hydroxy-6-methoxy-3,3-dimethyl-2,3-dihydro-1H-benzo[b]pyrano[3,2-h]-acridine-1,7(14H)-dione
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cc(C(=O)c2cc(F)cc(F)c2)ccc1F
Reaction #600116
title compound
Ausbeute 77.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCC[N+]1([O-])CCOCC1)Nc1nc2ccc(Sc3nnc4ccc(-c5ccc(F)cc5)nn34)cc2s1
Reaction #604994
white powder
Ausbeute 75.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(O)(CO)c1nc(Br)ccc1F
Reaction #625503
solid
Ausbeute 91.0%DOI: 10.6084/m9.figshare.5104873.v1
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