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792797

Fc1ccc2nnc(C3CCCCC3)n2c1
Reaction #162804
title compound
Ausbeute 31.2%DOI: 10.6084/m9.figshare.5104873.v1
N[C@H]1CC[C@@H](Oc2ccc3nnc(C4CCCCC4)n3c2)c2ccccc21
Reaction #162805
(1S,4R)-4-(3-Cyclohexyl-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy)-1,2,3,4-tetrahydro-naphthalen-1-ylamine
DOI: 10.6084/m9.figshare.5104873.v1
Fc1ccc2nnc(C3CCCCC3)n2c1
Reaction #659294
title compound
Ausbeute 31.2%DOI: 10.6084/m9.figshare.5104873.v1
N[C@H]1CC[C@@H](Oc2ccc3nnc(C4CCCCC4)n3c2)c2ccccc21
Reaction #659295
(1S,4R)-4-(3-Cyclohexyl-[1,2,4]triazolo[4,3-a]pyridin-6-yloxy)-1,2,3,4-tetrahydro-naphthalen-1-ylamine
DOI: 10.6084/m9.figshare.5104873.v1
CN1CCC[C@H]1c1nnc2ccc(O[C@@H]3CC[C@H](N)c4ccccc43)cn12
Reaction #717881
title compound
Ausbeute 36.8%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCC[C@@H]1c1nnc2ccc(O[C@@H]3CC[C@H](N)c4ccccc43)cn12
Reaction #717965
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CN1CCCC[C@H]1c1nnc2ccc(O[C@@H]3CC[C@H](N)c4ccccc43)cn12
Reaction #717968
title compound
Ausbeute 71.1%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(C)C(c2nnc3ccc(O[C@@H]4CC[C@H](N)c5ccccc54)cn23)C1
Reaction #718021
title compound
Ausbeute 66.2%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCC[C@H](c2nnc3ccc(F)cn23)C1
Reaction #718028
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CN1CCC[C@H](c2nnc3ccc(O[C@@H]4CC[C@H](N)c5ccccc54)cn23)C1
Reaction #718029
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CC[C@@H](c2nnc3ccc(F)cn23)C1
Reaction #718031
title compound
Ausbeute 73.0%DOI: 10.6084/m9.figshare.5104873.v1
Fc1ccc2nnc([C@@H]3CCNC3)n2c1
Reaction #718032
6-Fluoro-3-(R)-pyrrolidin-3-yl-[1,2,4]triazolo[4,3-a]pyridine
DOI: 10.6084/m9.figshare.5104873.v1
CN1CC[C@@H](c2nnc3ccc(F)cn23)C1
Reaction #718033
6-Fluoro-3-((R)-1-methyl-pyrrolidin-3-yl)-[1,2,4]triazolo[4,3-a]pyridine
DOI: 10.6084/m9.figshare.5104873.v1
CN1CC[C@@H](c2nnc3ccc(O[C@@H]4CC[C@H](N)c5ccccc54)cn23)C1
Reaction #718034
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CN1CCCC[C@H]1c1nnc2ccc(F)cn12
Reaction #718095
title compound
Ausbeute 42.0%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCCC[C@H]1c1nnc2ccc(O[C@@H]3CC[C@H](N)c4ccccc43)cn12
Reaction #718096
title compound
Ausbeute 45.3%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCC[C@H]1c1nnc2ccc(O[C@@H]3CC[C@H](N)c4ccccc43)cn12
Reaction #1489272
title compound
Ausbeute 36.8%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCC[C@H]1c1nnc2ccc(O[C@H]3C[C@H](N)c4ccccc43)cn12
Reaction #1489335
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CN1CCC[C@@H]1c1nnc2ccc(O[C@@H]3CC[C@H](N)c4ccccc43)cn12
Reaction #1489389
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CN1CCCC[C@H]1c1nnc2ccc(F)cn12
Reaction #1489394
title compound
Ausbeute 81.5%DOI: 10.6084/m9.figshare.5104873.v1
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