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1247730

COc1c(Cl)ccc(-c2cc(N)c(Cl)c(C(=O)NOC3CCCCO3)n2)c1F
Reaction #71523
powder
Ausbeute 69.7%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CCC[C@@H](C)[C@H]1CC[C@H]2[C@@H]3CCC4C[C@@H](OCc5cn(O[C@@H]6O[C@H](CO)[C@@H](O[C@@H]7O[C@H](CO)[C@H](O)[C@H](O)[C@H]7O)[C@H](O)[C@H]6O)nn5)CC[C@]4(C)[C@H]3CC[C@]12C
Reaction #162031
crude product
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CCC[C@@H](C)[C@H]1CC[C@H]2[C@@H]3CCC4C[C@@H](OCc5cn(O[C@@H]6O[C@H](CO)[C@@H](O[C@H]7O[C@H](CO)[C@@H](O)[C@H](O)[C@H]7O)[C@H](O)[C@H]6O)nn5)CC[C@]4(C)[C@H]3CC[C@]12C
Reaction #162032
off-white solid
Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(C=Cc1c[nH]c2ccccc12)NOC1CCCCO1
Reaction #171376
18
DOI: 10.6084/m9.figshare.5104873.v1
O=C(C=Cc1cn(S(=O)(=O)c2ccccc2)c2ccccc12)NOC1CCCCO1
Reaction #171377
19
Ausbeute 54.1%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
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
CC(CCn1ccc(-c2ccc(OCCCO)cc2)cc1=O)(C(=O)NOC1CCCCO1)S(C)(=O)=O
Reaction #171432
4-(4-(4-(3-hydroxypropoxy)phenyl)-2-oxopyridin-1(2H)-yl)-2-methyl-2-(methylsulfonyl)-N-(tetrahydro-2H-pyran-2-yloxy)butanamide
DOI: 10.6084/m9.figshare.5104873.v1
CC(CCn1ccc(-c2ccc(OCCCO)cc2)cc1=O)(C(=O)NO)S(C)(=O)=O
Reaction #171433
title compound
Ausbeute 20.6%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
Cc1c(-c2ccccc2)ccn(CCC(C)(C(=O)NOC2CCCCO2)S(C)(=O)=O)c1=O
Reaction #171460
2-methyl-4-(3-methyl-2-oxo-4-phenylpyridin-1(2H)-yl)-2-(methylsulfonyl)-N-(tetrahydro-2H-pyran-2-yloxy)butanamide
DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(-c2ccccc2)ccn(CCC(C)(C(=O)NO)S(C)(=O)=O)c1=O
Reaction #171461
N-hydroxy-2-methyl-4-(3-methyl-2-oxo-4-phenylpyridin-1(2H)-yl)-2-(methylsulfonyl)butanamide
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(COc2ccc(-c3ccn(CC[C@](C)(C(=O)NO)S(C)(=O)=O)c(=O)c3)cc2)cn1
Reaction #171485
(2R)-N-hydroxy-4-[4-{4-[(6-methoxypyridin-3-yl)methoxy]phenyl}-2-oxopyridin-1(2H)-yl]-2-methyl-2-(methylsulfonyl)butanamide
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@](CCn1ccc(-c2ccc(OC(F)(F)[C@H]3CC[C@H](O)CC3)cc2)cc1=O)(C(=O)NO)S(C)(=O)=O
Reaction #171489
(2R)-4-[4-{4-[difluoro(trans-4-hydroxycyclohexyl)methoxy]phenyl}-2-oxopyridin-1(2H)-yl]-N-hydroxy-2-methyl-2-(methylsulfonyl)butanamide
DOI: 10.6084/m9.figshare.5104873.v1
CC(CCn1ccc(OCCCC2CCCCC2)cc1=O)(C(=O)NOC1CCCCO1)S(C)(=O)=O
Reaction #171496
solid
Ausbeute 95.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(CCn1ccc(OCCCC2CCCCC2)cc1=O)(C(=O)NO)S(C)(=O)=O
Reaction #171497
solid
Ausbeute 54.4%DOI: 10.6084/m9.figshare.5104873.v1
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