Teilstruktursuche

S

CCN1CCCC1CNC(=O)c1cccc(CS(=O)(=O)C=C2CN(C(c3ccc(Cl)cc3)c3ccc(Cl)cc3)C2)c1
Reaction #53493
3-({1-[bis(4-chlorophenyl)methyl]azetidin-3-ylidene}methanesulfonylmethyl)-N-(1-ethylpyrrolidin-2-ylmethyl)benzamide
DOI: 10.6084/m9.figshare.5104873.v1
CCC(CC)CNC(=O)c1cccc(CS(=O)(=O)C=C2CN(C(c3ccc(Cl)cc3)c3ccc(Cl)cc3)C2)c1
Reaction #53499
3-({1-[bis(4-chlorophenyl)methyl]azetidin-3-ylidene}methanesulfonylmethyl)-N-(2-ethylbutyl)benzamide
Ausbeute 42.7%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)Cc1ccc(CS(=O)(=O)O)cc1
Reaction #54540
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cl)Cc1ccc(CS(=O)(=O)O)cc1
Reaction #54541
title compound
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cc(C23CO[C@@H](COCc4ccccc4)CC2CSC(NC(=O)c2ccccc2)=N3)c(F)cc1F
Reaction #155578
desired product
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cc([C@]23CO[C@@H](CF)C[C@H]2CSC(NC(=O)c2ccccc2)=N3)c(F)cc1F
Reaction #155581
N-[(4aR,6R,8aS)-8a-(5-cyano-2,4-difluorophenyl)-6-(fluoromethyl)-4,4a,5,6,8,8a-hexahydropyrano[3,4-d][1,3]thiazin-2-yl]benzamide
DOI: 10.6084/m9.figshare.5104873.v1
COC[C@H]1C[C@H]2CSC(NC(=O)c3ccccc3)=N[C@@]2(c2cc(C#N)c(F)cc2F)CO1
Reaction #155583
N-[(4aR,6R,8aS)-8a-(5-cyano-2,4-difluorophenyl)-6-(methoxymethyl)-4,4a,5,6,8,8a-hexahydropyrano[3,4-d][1,3]thiazin-2-yl]benzamide
DOI: 10.6084/m9.figshare.5104873.v1
COC(OC)C(C(OC)OC)[C@H]1C[C@H]2CSC(NC(=O)c3ccccc3)=N[C@@]2(c2cc(Br)ccc2F)CO1
Reaction #155608
product
DOI: 10.6084/m9.figshare.5104873.v1
Cn1cc([C@H]2C[C@H]3CSC(N)=N[C@@]3(c3cc(Br)ccc3F)CO2)cn1
Reaction #155609
(4aR,6R,8aS)-8a-(5-bromo-2-fluorophenyl)-6-(1-methyl-1H-pyrazol-4-yl)-4,4a,5,6,8,8a-hexahydropyrano[3,4-d][1,3]thiazin-2-amine
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1csc(-c2c(F)cccc2F)n1
Reaction #160781
ethyl 2-(2,6-difluorophenyl)thiazole-4-carboxylate
Ausbeute 84.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1csc(-c2c(F)cccc2F)n1
Reaction #160782
2-(2,6-difluorophenyl)thiazole-4-carboxylic acid
Ausbeute 88.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(COC(=O)CNC2=C(c3ccccc3)S(=O)(=O)N(C(C)(C)C)C2=O)cc1
Reaction #178150
DOI: 10.1039/C8SC04228D
COCCN1C(=O)C(Nc2cc(C3CCCCC3)ccc2OC)=C(c2ccccc2)S1(=O)=O
Reaction #179225
DOI: 10.1039/C8SC04228D
COCCN1C(=O)C(Nc2ccc(N3CCOCC3)cc2)=C(c2ccccc2)S1(=O)=O
Reaction #181149
DOI: 10.1039/C8SC04228D
CCC(CC)CNC(=O)c1cccc(CS(=O)(=O)C=C2CN(C(c3ccc(Cl)cc3)c3ccc(Cl)cc3)C2)c1
Reaction #181924
DOI: 10.1039/C8SC04228D
CS(=O)(=O)C(=C1CN(C(c2ccc(Cl)cc2)c2ccc(CN3CCCCC3)cc2)C1)c1cc(F)cc(F)c1
Reaction #182016
DOI: 10.1039/C8SC04228D
COc1cc(C=C2SC(NCCNC(=O)OC(C)(C)C)=NC2=O)ccc1Oc1ccc(C#N)cc1C(F)(F)F
Reaction #190036
DOI: 10.1039/C8SC04228D
O=Cc1nc(-c2ccccc2Cl)cs1
Reaction #193969
DOI: 10.1039/C8SC04228D
Cl
Reaction #200414
DOI: 10.1039/C8SC04228D
CC(C)(C)N1C(=O)C(NCC(c2ccccc2)c2ccccc2)=C(c2ccccc2)S1(=O)=O
Reaction #206209
DOI: 10.1039/C8SC04228D
ZurückSeite 2Weiter