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1223035

CNC(=O)C(Cc1ccc2ccccc2c1)N1CCNC(CCO[Si](C)(C)C(C)(C)C)C1=O
Reaction #8626
desired product
DOI: 10.6084/m9.figshare.5104873.v1
NCC(=O)N1CCN(c2cccc(CS(=O)(=O)C=C3CN(C(c4ccc(Cl)cc4)c4ccc(Cl)cc4)C3)c2)CC1
Reaction #53501
2-amino-1-{4-[3-({1-[bis-(4-chlorophenyl)methyl]azetidin-3-ylidene}methanesulfonylmethyl)phenyl]piperazin-1-yl}ethanone
Ausbeute 78.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NCC(=O)N1CCN(c2cccc(CS(=O)(=O)C=C3CN(C(c4ccc(Cl)cc4)c4ccc(Cl)cc4)C3)c2)CC1
Reaction #53502
(2-{4-[3-({1-[bis-(4-chlorophenyl)methyl]azetidin-3-ylidene}methanesulfonylmethyl)phenyl]piperazin-1-yl}-2-oxoethyl)carbamic acid tert-butyl ester
Ausbeute 102.2%DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)C1CN(CC(=O)Nc2c(Cl)cccc2Cl)CCN1CCCC(=O)C(c1ccccc1)c1ccccc1.O
Reaction #63624
3-(aminocarbonyl)-N-(2,6-dichlorophenyl)-4-(4-oxo-5,5-diphenylpentyl)-1-piperazineacetamide monohydrate
Ausbeute 3.7%DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2ccccc2CN1CC1(N2CCN(C3CC3)CC2)CCNCC1
Reaction #74278
desired product
Ausbeute 60.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(C)c(S(=O)(=O)N(CCOCC(=O)N2CCC(CN3Cc4ccccc4C3=O)(N3CCN(C4CC4)CC3)CC2)C2CC2)c(C)c1
Reaction #74283
crude product
Ausbeute 50.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc(-c2cnc3[nH]ccc3c2N2CCN(C(=O)[C@@H](Cc3ccc(Cl)cc3)NC(=O)OC(C)(C)C)CC2)c1
Reaction #166716
(R)-tert-butyl 3-(4-chlorophenyl)-1-(4-(5-(3-methoxyphenyl)-1H-pyrrolo[2,3-b]pyridin-4-yl)piperazin-1-yl)-1-oxopropan-2-ylcarbamate
Ausbeute 54.6%DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc(-c2cnc3[nH]ccc3c2N2CCN(C(=O)[C@H](N)Cc3ccc(Cl)cc3)CC2)c1
Reaction #166717
(R)-2-amino-3-(4-chlorophenyl)-1-(4-(5-(3-methoxyphenyl)-1H-pyrrolo[2,3-b]pyridin-4-yl)piperazin-1-yl)propan-1-one
Ausbeute 86.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(N2CCN(C(=O)Cn3nc(C(F)(F)F)c(Cl)c3C(C)O)CC2)ccc1Cl
Reaction #175287
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)NCCCCC(NC(=O)C(N)Cc1cc(Cl)c(O)c(Cl)c1)C(=O)N1CCN(c2ccncc2)CC1
Reaction #177823
DOI: 10.1039/C8SC04228D
CCC(CC)C(=O)Nc1ccc(N2CCN(C(C(=O)N(CC)CC)c3ccccc3)CC2)c(C#C[Si](C)(C)C)c1
Reaction #183673
DOI: 10.1039/C8SC04228D
O=C(NCC(=O)N1CCN(C(=O)c2cc(F)c(F)c(F)c2)CC1)c1ccc(-c2ccccc2)cc1
Reaction #187235
DOI: 10.1039/C8SC04228D
NCC(=O)N1CCN(c2cccc(CS(=O)(=O)C=C3CN(C(c4ccc(Cl)cc4)c4ccc(Cl)cc4)C3)c2)CC1
Reaction #195763
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)NCc1cc(Cl)c(NC(=O)CN2CCN(CCCCC(c3ccc(F)cc3)c3ccc(F)cc3)CC2C(N)=O)c(Cl)c1
Reaction #196096
DOI: 10.1039/C8SC04228D
CN1CCN(c2ccc(C(=O)NCC(=O)N3CCN(C(=O)c4cc(F)ccc4C(F)(F)F)CC3)cc2)CC1
Reaction #200486
DOI: 10.1039/C8SC04228D
CCCCCc1ccc(CN(C(=O)C=Cc2cccc(OC)c2)C(Cc2ccccc2)C(=O)N2CCN(Cc3ccccc3)CC2)cc1
Reaction #209680
DOI: 10.1039/C8SC04228D
CN1CCN(C(=O)Cn2cc(-c3cnc4[nH]cc(C(=O)C(C)(C)C)c4n3)c3ccccc32)CC1
Reaction #223485
DOI: 10.1039/C8SC04228D
Clc1ccc(C(c2ccccc2)N2CCN(CCNCc3cc(-c4ccccc4)n(-c4ccccc4)n3)CC2)cc1
Reaction #225291
DOI: 10.1039/C8SC04228D
O=C(NCC(=O)N1CCN(C(=O)c2ccccc2C(F)(F)F)CC1)c1ccco1
Reaction #226201
DOI: 10.1039/C8SC04228D
CCOCCn1c(CN2CCN(CCN=C=S)CC2)nc2cccnc21
Reaction #229731
DOI: 10.1039/C8SC04228D
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