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CCN(CC)CC.Cl

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
C[C@@H]1CN(Cc2ccc(F)cc2)[C@@H](C)CN1C(=O)COc1ccc(Cl)cc1S(N)(=O)=O
Reaction #11759
title compound
Выход 70.9%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)NC(=O)NS(=O)(=O)c1cc(Cl)ccc1OCC(=O)N1C[C@H](C)N(Cc2ccc(F)cc2)C[C@H]1C
Reaction #11760
title compound
Выход 72.1%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CN(Cc2ccc(F)cc2)[C@@H](C)CN1C(=O)COc1ccc(Cl)cc1S(=O)(=O)NC(=O)C(C)(C)C
Reaction #11761
title compound
Выход 49.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)OC(C)(C)C(=O)NS(=O)(=O)c1cc(Cl)ccc1OCC(=O)N1C[C@H](C)N(Cc2ccc(F)cc2)C[C@H]1C
Reaction #11762
crude title compound
Выход 111.5%DOI: 10.6084/m9.figshare.5104873.v1
Cl.O=c1[nH]c(=O)n(CCCCN2C[C@@H]3C[C@]3(c3ccc(C(F)(F)F)cc3)C2)cc1C(F)(F)F
Reaction #41036
title compound
Выход 76.0%DOI: 10.6084/m9.figshare.5104873.v1
Cl.O=c1[nH]c(=O)n(CCCCN2C[C@@H]3C[C@]3(c3ccc(C(F)(F)F)cc3)C2)cc1C(F)(F)F
Reaction #41037
title compound
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
Выход 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
Выход 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
Выход 74.8%DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc(OC2=CC(=O)N([C@@H](CC3CCCC3)C(=O)Nc3ccn(CC(C)(C)O)n3)C2)c1Cl
Reaction #47265
(S)-2-[4-(2-chloro-3-methoxy-phenoxy)-2-oxo-2,5-dihydro-pyrrol-1-yl]-3-cyclopentyl-N-[1-(2-hydroxy-2-methyl-propyl)-1H-pyrazol-3-yl]-propionamide
Выход 54.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C[C@@H](C(=O)Nc1ccn(C)n1)N1CC(Oc2cccc(Cl)c2Cl)=CC1=O
Reaction #47293
(S)-2-[4-(2,3-dichloro-phenoxy)-2-oxo-2,5-dihydro-pyrrol-1-yl]-4-methyl-pentanoic acid (1-methyl-1H-pyrazol-3-yl)-amide
DOI: 10.6084/m9.figshare.5104873.v1
CCO[C@H](C)C[C@@H](C(=O)Nc1ccn(CC(C)(C)O)n1)N1CC(Oc2cccc(Cl)c2Cl)=CC1=O
Reaction #47319
(2S,4R)-2-[4-(2,3-dichloro-phenoxy)-2-oxo-2,5-dihydro-pyrrol-1-yl]-4-ethoxy-pentanoic acid [1-(2-hydroxy-2-methyl-propyl)-1H-pyrazol-3-yl]-amide
Выход 32.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C[C@@H](C(=O)Nc1ccn(C[C@@H]2CNC(=O)O2)n1)N1CC(Oc2ccccc2Cl)=CC1=O
Reaction #47467
(S)-2-[4-(2-chloro-phenoxy)-2-oxo-2,5-dihydro-pyrrol-1-yl]-4-methyl-pentanoic acid [1-((S)-2-oxo-oxazolidin-5-ylmethyl)-1H-pyrazol-3-yl]-amide
Выход 58.3%DOI: 10.6084/m9.figshare.5104873.v1
CCC(C)C[C@@H](C(=O)Nc1ccn(C[C@@H](O)CO)n1)N1CC(Oc2ccccc2Cl)=CC1=O
Reaction #47688
(S)-2-[4-(2-chloro-phenoxy)-2-oxo-2,5-dihydro-pyrrol-1-yl]-4-methyl-hexanoic acid [1-((R)-2,3-dihydroxy-propyl)-1H-pyrazol-3-yl]-amide
Выход 86.0%DOI: 10.6084/m9.figshare.5104873.v1
CCc1cc(CCN(Cc2ccc(C(C)(C)C)cc2)C(=O)c2cc(C(F)(F)F)cc(Cl)c2F)ccc1F
Reaction #48092
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(CCS(=O)(=O)c1ccc2cc(Cl)ccc2c1)N1CCC(N2CCCC2=O)CC1
Reaction #48493
title compound
Выход 39.0%DOI: 10.6084/m9.figshare.5104873.v1
Cl.Cl.O=c1c(-c2cccnc2)c[nH]n1-c1cc(N2CCC(N3CCCC3)CC2)ncn1
Reaction #66180
4-Pyridin-3-yl-2-[6-(4-pyrrolidin-1-ylpiperidin-1-yl)pyrimidin-4-yl]-1,2-dihydro-3H-pyrazol-3-one dihydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
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