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1137352

CS(=O)(=O)CCN1C[C@H](c2cccc(F)c2F)CC[C@@H](NC(=O)N2CCC(n3c(=O)[nH]c4ncccc43)CC2)C1=O
Reaction #48437
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCn1cc(-c2ccnc3[nH]c(-c4ccc(CN5CCOCC5)cc4)cc23)c(-c2ccc(NC(=O)N3CCS(=O)(=O)CC3)cc2)n1
Reaction #57172
title product
Ausbeute 30.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc2c(ncn2CCS(C)(=O)=O)c(F)c1Nc1ccc(Br)cc1Cl
Reaction #60280
pure desired product
Ausbeute 59.1%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)CCn1cnc2c(F)c(Nc3ccc(Br)cc3Cl)c(CO)cc21
Reaction #60303
clean desired product
Ausbeute 79.5%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)CCn1cnc2c(F)c(Nc3ccc(Br)cc3Cl)c(C=O)cc21
Reaction #60304
desired product
Ausbeute 82.3%DOI: 10.6084/m9.figshare.5104873.v1
Fc1c(Nc2ccc(Br)cc2Cl)c(-c2cnco2)cc2[nH]cnc12
Reaction #60305
desired product 10
Ausbeute 18.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)C2N=COC2c2cc3c(ncn3CCS(C)(=O)=O)c(F)c2Nc2ccc(Br)cc2Cl)cc1
Reaction #60306
(4-Bromo-2-chloro-phenyl)-{4-fluoro-1-(2-methanesulfonyl-ethyl)-6-[4-(toluene-4-sulfonyl)-4,5-dihydro-oxazol-5-yl]-1H-benzoimidazol-5-yl}-amine
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CC(C(N)=O)S(C)(=O)=O)cc1C(=O)NCc1ccc(C(F)(F)F)cc1
Reaction #77810
aimed product
Ausbeute 70.8%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)N1CCC[C@@]1(C[C@@H](O)[C@H](Cc1ccccc1)NC(=O)[C@H](CS(C)(=O)=O)NC(=O)OCc1ccccc1)C(=O)[NH2+][O-].N#N.O
Reaction #82370
N2 [3(S)-[[N-(benzyloxycarbonyl)-3-(methylsulphonyl)-L-alanyl]amino]-2(R)-hydroxy-4-phenylbutyl]-N1 -tert.butyl-L-prolinamide N2 -oxide monohydrate
Ausbeute 34.5%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@](CCn1ccc(-c2ccc(-n3cccn3)cc2)cc1=O)(C(=O)NO)S(C)(=O)=O
Reaction #171398
solid
Ausbeute 99.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(CCn1ccc(-c2ccc(OCCCN3CCC(F)(F)CC3)cc2)cc1=O)(C(=O)NO)S(C)(=O)=O.Cl
Reaction #171404
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@](CCn1ccc(-c2ccc(OC[C@H]3CC[C@@H](O)CC3)cc2)cc1=O)(C(=O)NO)S(C)(=O)=O
Reaction #171412
title compound
Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@](CCn1ccc(-c2ccc(OC[C@H]3CC[C@H](OC4CCCCO4)CC3)cc2)cc1=O)(C(=O)NOC1CCCCO1)S(C)(=O)=O
Reaction #171415
title compound
Ausbeute 49.7%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@](CCn1ccc(-c2ccc(OC[C@H]3CC[C@H](O)CC3)cc2)cc1=O)(C(=O)NO)S(C)(=O)=O
Reaction #171416
title compound
Ausbeute 83.9%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@](CCn1ccc(-c2ccc(OC[C@H]3CC[C@H](OC4CCCCO4)CC3)cc2F)cc1=O)(C(=O)NOC1CCCCO1)S(C)(=O)=O
Reaction #171418
title compound
Ausbeute 795.9%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #171421
solid
Ausbeute 92.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(O)ccc(-c2ccn(CC[C@](C)(C(=O)NO)S(C)(=O)=O)c(=O)c2)c1F
Reaction #171424
white solid
Ausbeute 6.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@](CCn1ccc(-c2ccc(OCCC3CC(O)C3)cc2)cc1=O)(C(=O)NO)S(C)(=O)=O
Reaction #171439
title compound
Ausbeute 80.5%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@](CCn1ccc(-c2ccc(Cl)c(F)c2F)cc1=O)(C(=O)NO)S(C)(=O)=O
Reaction #171451
title compound
Ausbeute 48.7%DOI: 10.6084/m9.figshare.5104873.v1
CC(CCn1ccc(OCc2ccccc2)cc1=O)(C(=O)NO)S(C)(=O)=O
Reaction #171455
title compound
Ausbeute 26.7%DOI: 10.6084/m9.figshare.5104873.v1
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