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580567

CC(C)NC(=O)OCc1ccc2c(n1)N1[C@H](C2)CN(C(=O)OC(C)(C)C)C[C@H]1C
Reaction #12056
title compound
Ausbeute 436.7%DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCC2N1CC(=O)N2Cc1ccccc1
Reaction #43391
title compound
Ausbeute 87.0%DOI: 10.6084/m9.figshare.5104873.v1
COC[C@H](C)Oc1cc(Oc2ccc(C(C)=O)cc2)cc(C(=O)Nc2ccn(C)n2)c1
Reaction #48874
desired product
Ausbeute 49.8%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(Oc2nn(-c3ccccc3F)c3cccc(F)c23)CC1
Reaction #58691
Intermediate 46
Ausbeute 51.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccc(-c2cnco2)cc1)N(C1CC1)C1CCN(c2ncc(C3CC3)cn2)CC1
Reaction #156065
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COCCn1c(=O)n(C(C)c2ccccn2)c2c3cc(OC)c(-c4c(C)noc4C)cc3ncc21
Reaction #175459
DOI: 10.1039/C8SC04228D
CC(NC(=O)c1cc(Cl)cnc1Oc1cccc(-c2nccs2)c1)c1ccc(C(=O)OC(C)(C)C)cc1
Reaction #205555
DOI: 10.1039/C8SC04228D
COc1cccc(-c2nc3ncc(-c4ccccc4)cc3n2Cc2ccc(F)cc2)c1
Reaction #225209
DOI: 10.1039/C8SC04228D
CCC(=O)Nc1nc2c(Oc3cc(-c4ccc(C(F)(F)F)cc4)ncn3)cccc2s1
Reaction #228258
DOI: 10.1039/C8SC04228D
O=C(Cc1ccccc1)Nc1nc2c(Oc3cc(-c4ccc(C(F)(F)F)cc4)ncn3)cccc2s1
Reaction #230277
DOI: 10.1039/C8SC04228D
COC(=O)c1c(-c2ccccc2)c2cc(Br)ccc2c(=O)n1Cc1ccccc1F
Reaction #248453
DOI: 10.1039/C8SC04228D
CC(C)(C)N1C(=O)C(NC2CCN(C(=O)c3ccccc3C(F)(F)F)CC2)=C(c2ccccc2)S1(=O)=O
Reaction #251669
DOI: 10.1039/C8SC04228D
COc1ccc(CCNc2cc(-c3nnc(C)o3)nc(OC)n2)cc1
Reaction #303348
[2-methoxy-6-(5-methyl-[1,3,4]oxadiazol-2-yl)-pyrimidin-4-yl]-[2-(4-methoxy-phenyl)-ethyl]-amine
Ausbeute 63.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc2c(C3CCCCC3)c3n(c2c1)C(O)c1ccccc1-3
Reaction #359729
title compound
Ausbeute 69.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CS(=O)(=O)N1CCOCC1
Reaction #359730
title compound
Ausbeute 71.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CS(=O)(=O)N1CCOCC1
Reaction #359731
title compound
Ausbeute 64.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CS(=O)(=O)N1CCOCC1
Reaction #359732
title compound
Ausbeute 68.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CS(=O)(=O)N1CCN(C)CC1
Reaction #359733
title compound
Ausbeute 68.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CS(=O)(=O)N1CCN(C)CC1
Reaction #359734
title compound
Ausbeute 52.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(Cl)c(N2CCN(C(=O)c3c(-c4ccccc4OC)noc3C)CC2)cc1NC(=O)c1ccc(N(C)C)cc1
Reaction #369861
DOI: 10.1039/C8SC04228D
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