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766716

Cl.Cl.Nc1ccc(N2CCC[C@@H](C(=O)N3CCCC3)C2)nc1N
Reaction #1018236
title compound
Ausbeute 99.7%DOI: 10.6084/m9.figshare.5104873.v1
Nc1nc(N2CCC[C@@H](C(=O)N3CCCC3)C2)ncc1[N+](=O)[O-]
Reaction #1018241
(R)-(1-(4-amino-5-nitropyrimidin-2-yl)piperidin-3-yl)(pyrrolidin-1-yl)methanone
DOI: 10.6084/m9.figshare.5104873.v1
Cl.Cl.Nc1ccc(N2CCC[C@@H](C(=O)N3CCC(F)(F)C3)C2)nc1N
Reaction #1018277
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cl.Cl.Nc1ccc(N2CCC[C@@H](C(=O)N3CC[C@H](O)C3)C2)nc1N
Reaction #1018278
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cl.Cl.Nc1ccc(N2CCO[C@@H](C(=O)N3CCCC3)C2)nc1N
Reaction #1018287
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Nc1nc(N2CCC[C@@H](C(=O)N3CCCC3)C2)ccc1NC(=O)C1(c2cccnc2)CC1
Reaction #1018383
(R)—N-(2-amino-6-(3-(pyrrolidine-1-carbonyl)piperidin-1-yl)pyridin-3-yl)-1-(pyridin-3-yl)cyclopropanecarboxamide
Ausbeute 84.5%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(C2(C(=O)Nc3ccc(N4CCC[C@@H](C(=O)N5CCCC5)C4)nc3N)CC2)on1
Reaction #1018385
(R)—N-(2-amino-6-(3-(pyrrolidine-1-carbonyl)piperidin-1-yl)pyridine-3-yl)-1-(3-methylisoxazol-5-yl)cyclopropanecarboxamide
Ausbeute 53.2%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccn(C2(C(=O)Nc3ccc(N4CCC[C@@H](C(=O)N5CCCC5)C4)nc3N)CC2)n1
Reaction #1018387
(R)—N-(2-amino-6-(3-(pyrrolidine-1-carbonyl)piperidin-1-yl)pyridin-3-yl)-1-(3-methyl-1H-pyrazol-1-yl)cyclopropanecarboxamide
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccccc1C1(c2nc3ccc(N4CCC[C@@H](C(=O)N5CCCC5)C4)nc3[nH]2)CC1
Reaction #1018389
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C([C@@H]1CCCN(c2ccc3nc(-c4ccnc(C5CC5)n4)[nH]c3n2)C1)N1CCCC1
Reaction #1018390
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc(C2(c3nc4ccc(N5CCC[C@@H](C(=O)N6CCCC6)C5)nc4[nH]3)CC2)c1
Reaction #1018391
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(C2(c3nc4ccc(N5CCC[C@@H](C(=O)N6CCCC6)C5)nc4[nH]3)CC2)cc1
Reaction #1018392
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cn1nccc1C1(c2nc3ccc(N4CCC[C@@H](C(=O)N5CCCC5)C4)nc3[nH]2)CC1
Reaction #1018393
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cc(CC)nc(-c2nc3ccc(N4CCC[C@@H](C(=O)N5CCCC5)C4)nc3[nH]2)c1
Reaction #1018394
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C([C@@H]1CCCN(c2ccc3nc(-c4cncc(C5CC5)n4)[nH]c3n2)C1)N1CCOCC1
Reaction #1018395
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C([C@@H]1CCCN(c2ccc3nc(C4(n5cc(Cl)cn5)CC4)[nH]c3n2)C1)N1CCCC1
Reaction #1018396
(R)-(1-(2-(1-(4-chloro-1H-pyrazol-1-yl)cyclopropyl)-3H-imidazo[4,5-b]pyridin-5-yl)piperidin-3-yl)(pyrrolidin-1-yl)methanone
Ausbeute 94.7%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)Cc1cccc(-c2nc3ccc(N4CCC[C@@H](C(=O)N5CCCC5)C4)nc3[nH]2)c1
Reaction #1018403
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C([C@@H]1CCCN(c2ccc3nc(-c4cccc(C5(O)COC5)n4)[nH]c3n2)C1)N1CCCC1
Reaction #1018404
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C([C@@H]1CCCN(c2ccc3nc(-c4cccc(C(F)(F)F)n4)[nH]c3n2)C1)N1CCCC1
Reaction #1018405
title compound
Ausbeute 29.0%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)c1cccc(-c2nc3ccc(N4CCC[C@@H](C(=O)N5CCCC5)C4)nc3[nH]2)c1
Reaction #1018408
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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