Recherche de Sous-structure

31234

Cl.O=C1Cc2cc(CCN3CCN(c4nsc5ccccc45)CC3)c(Cl)cc2N1
Reaction #7690
5-[2-[4-(1,2-benzisothiazol-3-yl)-1-piperazinyl]ethyl]-6-chloro-1, 3-dihydro-2H-indol-2-one hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
Cl.O=C1Cc2cc(CCN3CCN(c4nsc5ccccc45)CC3)c(Cl)cc2N1
Reaction #7691
5-[2-[4-(1,2-benzisothiazol-3-yl)-1-piperazinyl]ethyl]-6-chloro-1, 3-dihydro-2H-indol-2-one hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
Cl.O=C1Cc2cc(CCN3CCN(c4nsc5ccccc45)CC3)c(Cl)cc2N1
Reaction #7692
5-[2-[4-(1,2-benzisothiazol-3-yl)-1-piperazinyl]ethyl]-6-chloro-1, 3-dihydro-2H-indol-2-one hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
O=C1Cc2cc(CCN3CCN(c4nsc5ccccc45)CC3)c(Cl)cc2N1
Reaction #41843
5-(2-(4-(1,2-benzisothiazol-3-yl)-1-piperazinyl)ethyl)-6-chloro-1,3-dihydro-2H-indol-2-one
Rendement 75.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1Cc2cc(CCN3CCN(c4nsc5ccccc45)CC3)c(Cl)cc2N1
Reaction #41844
5-(2-(4-(1,2-benzisothiazol-3-yl)-1-piperazinyl)ethyl)-6-chloro-1,3-dihydro-2H-indol-2-one
Rendement 75.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1Cc2cc(CCN3CCN(c4nsc5ccccc45)CC3)c(Cl)cc2N1
Reaction #41845
5-(2-(4-(1,2-benzisothiazol-3-yl)-1-piperazinyl)ethyl)-6-chloro-1,3-dihydro-2H-indol-2-one
Rendement 74.8%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)Oc1ccc(S(C)(=O)=O)cc1C(=O)N1CCN(c2nsc3ccccc23)CC1
Reaction #61461
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCN(CC)c1ccc(S(C)(=O)=O)cc1C(=O)N1CCN(c2nsc3ccccc23)CC1
Reaction #61462
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1cc([N+](=O)[O-])ccc1N1CCOCC1)N1CCN(c2nsc3ccccc23)CC1
Reaction #61463
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)c1ccc(OCC2CC2)c(C(=O)N2CCN(c3nsc4ccccc34)CC2)c1
Reaction #61464
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](Oc1ccc(S(C)(=O)=O)cc1C(=O)N1CCN(c2nsc3ccccc23)CC1)C(F)(F)F
Reaction #61465
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(C(C)=O)ccc1OCCCCN1CCN(c2nsc3ccccc23)CC1
Reaction #83860
1-[4-[4-[4-(1,2-benzisothiazol-3-yl)-1-piperazinyl]butoxy]-3-methoxyphenyl]ethanone
Rendement 39.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)SCN(CCCCN2CCN(c3nsc4ccccc34)CC2)C1=O
Reaction #179880
DOI: 10.1039/C8SC04228D
CC(=O)Nc1ccc(F)cc1CCN1CCN(c2nsc3ccccc23)CC1
Reaction #180166
DOI: 10.1039/C8SC04228D
CCCC1(C)CC(=O)N(CCCCN2CCN(c3nsc4ccccc34)CC2)C(=O)C1
Reaction #180181
DOI: 10.1039/C8SC04228D
O=C(Nc1ccc(CCN2CCN(c3nsc4ccccc34)CC2)cc1)c1cnccn1
Reaction #181180
DOI: 10.1039/C8SC04228D
O=C1Cc2cc(CCN3CCN(c4nsc5ccccc45)CC3)c(Cl)cc2N1
Reaction #182827
DOI: 10.1039/C8SC04228D
O=[N+]([O-])c1ccc(OCCN2CCN(c3nsc4ccccc34)CC2)cc1
Reaction #184676
DOI: 10.1039/C8SC04228D
c1ccc2c(N3CCNCC3)nsc2c1
Reaction #186805
DOI: 10.1039/C8SC04228D
CC(=O)N1CCc2c(sc(C)c2CCN2CCN(c3nsc4ccccc34)CC2)C1
Reaction #187518
DOI: 10.1039/C8SC04228D
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