Recherche de Sous-structure

6254

C[C@H](CN1CCN(c2cccc3[nH]ccc23)CC1)Nc1ccccn1
Reaction #991
(R)-1-(4-indolyl)-4-[2-methyl-2-(2-pyridinylamino)ethyl]piperazine
Rendement 67.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCN(c2cccc3c2ccn3[Si](C)(C)C(C)(C)C)CC1
Reaction #8412
N-tert-Butyldimethylsilyl-4-(4-Boc-piperazinyl)-indole
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(C)c(S(=O)(=O)n2ccc3c(N4CCNCC4)cccc32)c(C)c1.Cl
Reaction #8413
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cl.O=S(=O)(c1cccc2ccccc12)n1ccc2c(N3CCNCC3)cccc21
Reaction #8414
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cl.O=S(=O)(c1cc(Cl)sc1Cl)n1ccc2c(N3CCNCC3)cccc21
Reaction #8415
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(S(=O)(=O)n2ccc3c(N4CCNCC4)cccc32)cc1.Cl
Reaction #8416
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cl.O=S(=O)(c1ccc(F)cc1F)n1ccc2c(N3CCNCC3)cccc21
Reaction #8417
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cl.O=S(=O)(c1ccc(-c2ccccc2)cc1)n1ccc2c(N3CCNCC3)cccc21
Reaction #8418
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(S(=O)(=O)n2ccc3c(N4CCNCC4)cccc32)cc1OC.Cl
Reaction #8419
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cl.O=S(=O)(c1cc(Cl)ccc1Cl)n1ccc2c(N3CCNCC3)cccc21
Reaction #8420
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1nn(C)c(Cl)c1S(=O)(=O)n1ccc2c(N3CCNCC3)cccc21.Cl
Reaction #8421
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cl.O=S(=O)(c1cccnc1)n1ccc2c(N3CCNCC3)cccc21
Reaction #8422
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)c1ccccc1S(=O)(=O)n1ccc2c(N3CCNCC3)cccc21.Cl
Reaction #8423
title compound
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #8424
hydrochloride salt
Rendement 45.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)n2ccc3c(N4CCN(C)CC4)cccc32)cc1.Cl
Reaction #8425
title compound
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #8428
white solid
Rendement 12.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccccc1S(=O)(=O)n1ccc2c(N3CCNC(C)C3)cccc21
Reaction #8429
white solid
Rendement 38.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #8431
white solid
Rendement 48.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCN(c2cccc3c2cc(I)n3S(=O)(=O)c2ccccc2)CC1
Reaction #8436
tert-Butyl 4-[2-iodo-1-(phenylsulfonyl)-1H-indol-4-yl]-1-piperazinecarboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCN(c2cccc3c2cc(-c2ccccc2)n3S(=O)(=O)c2ccccc2)CC1
Reaction #8437
tert-Butyl 4-[2-phenyl-1-(phenylsulfonyl)-1H-indol-4-yl]-1-piperazinecarboxylate
DOI: 10.6084/m9.figshare.5104873.v1
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