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446261

CS(=O)(=O)c1ccccc1S(=O)(=O)Nc1ccc2[nH]nc(-c3ccccc3[N+](=O)[O-])c2c1
Reaction #53687
N-[3-(2-nitrophenyl)-1H-indazol-5-yl]-2-methylsulfonylbenzenesulfonamide
Ausbeute 16.2%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)c1ccccc1S(=O)(=O)Nc1ccc2[nH]nc(-c3cccs3)c2c1
Reaction #53688
2-methylsulfonyl-N-(3-thiophen-2-yl-1H-indazol-5-yl)benzenesulfonamide
Ausbeute 36.5%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)c1ccccc1S(=O)(=O)Nc1ccc2[nH]nc(-c3ccsc3)c2c1
Reaction #53689
2-methylsulfonyl-N-(3-thiophen-3-yl-1H-indazol-5-yl)benzenesulfonamide
Ausbeute 16.9%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)c1ccccc1S(=O)(=O)Nc1ccc2[nH]nc(-c3ccoc3)c2c1
Reaction #53690
N-(3-furan-3-yl-1H-indazol-5-yl)-2-methylsulfonylbenzenesulfonamide
Ausbeute 35.7%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)c1ccccc1S(=O)(=O)Nc1ccc2[nH]nc(-c3ccco3)c2c1
Reaction #53691
N-(3-furan-2-yl-1 H-indazol-5-yl)-2-methylsulfonylbenzenesulfonamide
Ausbeute 32.5%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)c1ccccc1S(=O)(=O)Nc1ccc2[nH]nc(-c3ccncc3)c2c1
Reaction #53692
2-methylsulfonyl-N-(3-pyridin-4-yl-1H-indazol-5-yl)benzenesulfonamide
Ausbeute 15.8%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)c1ccccc1S(=O)(=O)Nc1ccc2[nH]nc(-c3cc4cccnc4[nH]3)c2c1
Reaction #53693
2-methylsulfonyl-N-[3-(1H-pyrrolo[2,3-b]pyridin-2-yl)-1H-indazol-5-yl]benzenesulfonamide
Ausbeute 45.9%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2[nH]c(-c3n[nH]c4ccc(NS(=O)(=O)c5ccccc5S(C)(=O)=O)cc34)cc2c1
Reaction #53694
2-methylsulfonyl-N-[3-(5-methoxy-1H-indol-2-yl)-1H-indazol-5-yl]benzenesulfonamide
Ausbeute 19.3%DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(Nc1ccc2[nH]nc(-c3cc4ccccc4[nH]3)c2c1)c1ccccc1
Reaction #53715
N-[3-(1H-indol-2-yl)-1H-indazol-5-yl]benzenesulfonamide
Ausbeute 66.3%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)c1ccccc1S(=O)(=O)Nc1ccc2[nH]nc(Nc3ccccc3)c2c1
Reaction #53716
2-methylsulfonyl-N-(3-phenylamino-1H-indazol-5-yl)benzenesulfonamide
Ausbeute 47.5%DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(Nc1ccc2[nH]nc(-c3cc4ccccc4[nH]3)c2c1)c1cccs1
Reaction #53718
solid
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1c(-c2ccc(F)cc2)nn2cc(NS(C)(=O)=O)c(OCc3ccccc3)cc12
Reaction #72390
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(c2cc(Cl)ccc2Oc2cc(F)c(S(=O)(=O)N(C(=O)OC(C)(C)C)c3cscn3)cc2Cl)CC1
Reaction #74510
tert-butyl 4-[2-(4-{[(tert-butoxycarbonyl)(1,3-thiazol-4-yl)amino]sulfonyl}-2-chloro-5-fluorophenoxy)-5-chlorophenyl]piperidine-1-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cc(S(=O)(=O)Nc2cscn2)ccc1Oc1ccc(Cl)cc1-c1ccnn1C1CNC1
Reaction #74532
powder
Ausbeute 38.9%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N(c1cscn1)S(=O)(=O)c1ccc(F)c(C#N)c1
Reaction #74597
title compound
Ausbeute 54.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N(c1cscn1)S(=O)(=O)c1ccc(Oc2ccc(Cl)cc2I)c(C#N)c1
Reaction #74598
title compound
Ausbeute 100.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N(c1cscn1)S(=O)(=O)c1ccc(Oc2ccc(Cl)cc2-c2ccnn2C2CNC2)c(C#N)c1
Reaction #74630
crude title compound
DOI: 10.6084/m9.figshare.5104873.v1
CN(C(=O)OC(C)(C)C)S(=O)(=O)c1ccsc1C(=O)O[C@@H](Cc1c(Cl)c[n+]([O-])cc1Cl)c1ccc(OC(F)F)c(OCC2CC2)c1
Reaction #88013
(S)-4-(2-(3-(N-(tert-butoxycarbonyl)-N-methylsulfamoyl)thiophene-2-carbonyloxy)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy) phenyl)ethyl)-3,5-dichloropyridine 1-oxide
Ausbeute 68.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N(c1csc(C(=O)O)c1)S(C)(=O)=O
Reaction #88019
4-(N-(tert-butoxycarbonyl)-methylsulfonamido)thiophene-2-carboxylic acid
Ausbeute 79.7%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N(c1csc(C(=O)O[C@@H](Cc2c(Cl)c[n+]([O-])cc2Cl)c2ccc(OC(F)F)c(OCC3CC3)c2)c1)S(C)(=O)=O
Reaction #88020
(S)-4-(2-(4-(N-(tert-butoxycarbonyl)methylsulfonamido)thiophene-2-carbonyloxy)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)ethyl)-3,5-dichloropyridine 1-oxide
Ausbeute 32.2%DOI: 10.6084/m9.figshare.5104873.v1
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