Teilstruktursuche

760350

N#Cc1ncc2c(c1O)c1cc(Cl)cnc1n2S(=O)(=O)c1ccccc1
Reaction #88510
title compound
Ausbeute 27.7%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ncc2c(c1Cl)c1cc(Cl)cnc1n2S(=O)(=O)c1ccccc1
Reaction #88511
title compound
Ausbeute 59.0%DOI: 10.6084/m9.figshare.5104873.v1
C[Si](C)(C)CCOCn1c2cnc(C#N)cc2c2c(N3CC[C@H](O)C3)c(Cl)cnc21
Reaction #88549
title compound
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cc2c(cn1)[nH]c1ncc(Cl)c(N3CC[C@H](O)C3)c12
Reaction #88550
title compound
Ausbeute 63.7%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)n2cc(-c3ncc(F)c(N[C@H]4CCCNC4)n3)c3cc(Cl)cnc32)cc1
Reaction #162045
desired product ( 1c )
DOI: 10.6084/m9.figshare.5104873.v1
COC([C@H](C)O)N1CCCCC1Nc1nc(-c2cn(S(=O)(=O)c3ccc(C)cc3)c3ncc(Cl)cc23)ncc1F
Reaction #162046
desired product ( 1d )
DOI: 10.6084/m9.figshare.5104873.v1
COC([C@H](C)O)N1CCCCC1Nc1nc(-c2c[nH]c3ncc(Cl)cc23)ncc1F
Reaction #162047
desired product ( 537 )
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)n2cc(-c3ncc(F)c(N[C@H]4CCCN(CC(F)(F)F)C4)n3)c3cc(Cl)cnc32)cc1
Reaction #162048
3a
DOI: 10.6084/m9.figshare.5104873.v1
Fc1cnc(-c2c[nH]c3ncc(Cl)cc23)nc1N[C@H]1CCCN(CC(F)(F)F)C1
Reaction #162049
desired product
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)n2cc(-c3ncc(F)c(N[C@H]4CCCN(Cc5ncc[nH]5)C4)n3)c3cc(Cl)cnc32)cc1
Reaction #162050
4a
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C=O)CC1N1CCCCC1Nc1nc(-c2c[nH]c3ncc(Cl)cc23)ncc1F
Reaction #162060
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CCCS(=O)(=O)N1CC(Nc2nc(-c3cn(S(=O)(=O)c4ccc(C)cc4)c4ncc(Cl)cc34)ncc2F)C1
Reaction #162063
desired product
Ausbeute 43.0%DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(CC1CCCC1)N1CC(Nc2nc(-c3c[nH]c4ncc(Cl)cc34)ncc2F)C1
Reaction #162064
desired product
Ausbeute 88.0%DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)N1CCC1Nc1nc(-c2c[nH]c3ncc(Cl)cc23)ncc1F
Reaction #162065
512
Ausbeute 79.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)n2cc(-c3ncc(F)c(N[C@H]4CCNC4)n3)c3cc(Cl)cnc32)cc1
Reaction #162067
7c
Ausbeute 88.0%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)N1CC[C@H](Nc2nc(-c3c[nH]c4ncc(Cl)cc34)ncc2F)C1
Reaction #162068
398
Ausbeute 37.0%DOI: 10.6084/m9.figshare.5104873.v1
CCS(=O)(=O)N1CC[C@H](Nc2nc(-c3c[nH]c4ncc(Cl)cc34)ncc2F)C1
Reaction #162069
399
Ausbeute 49.0%DOI: 10.6084/m9.figshare.5104873.v1
COCCC(=O)N1CCC[C@H](CNc2nc(-c3c[nH]c4ncc(Cl)cc34)ncc2F)C1
Reaction #162078
desired product
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)n2cc(-c3ncc(F)c(NCC4CC(F)(F)CCN4C(=O)OC(C)(C)C)n3)c3cc(Cl)cnc32)cc1
Reaction #162086
13j
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(F)(F)CC1CNc1nc(-c2c[nH]c3ncc(Cl)cc23)ncc1F
Reaction #162087
tert-butyl 2-((2-(5-chloro-1H-pyrrolo[2,3-b]pyridin-3-yl)-5-fluoropyrimidin-4-ylamino)methyl)-4,4-difluoropiperidine-1-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
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