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C1CCC(C(C1)N)N

CC(C)(C)OC(=O)N1C(NCc2ccc(F)cc2)=N[C@@H]2CCCC[C@@H]21
Reaction #47026
product 193
Ausbeute 98.1%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)[C@@H]1CCCC[C@H]1NC(=O)c1cccc(C(F)(F)F)c1.Cc1ccc(S(=O)(=O)O)cc1
Reaction #54534
amide
Ausbeute 47.0%DOI: 10.6084/m9.figshare.5104873.v1
Br.NCC(=O)N[C@H]1CCCC[C@H]1NC(=O)c1ccc(S(N)(=O)=O)cc1
Reaction #77832
N-(cis)-{2-[(aminoacetyl)amino]cyclohexyl}-4-(aminosulfonyl)benzamide hydrogen bromide
DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)c1ccccc1.Nc1ccc(I)cc1C(=O)NCC(=O)N[C@@H]1CCCC[C@@H]1NC(=O)c1ccc(S(N)(=O)=O)cc1
Reaction #77833
benzamide 2-amino-N-{2-[((cis)-2-{[4-(aminosulfonyl)benzoyl]amino}cyclohexyl)amino]-2-oxoethyl}-5-iodobenzamide
Ausbeute 12.3%DOI: 10.6084/m9.figshare.5104873.v1
NS(=O)(=O)c1ccc(C(=O)N[C@@H]2CCCC[C@@H]2NC(=O)CNC(=O)Nc2ccccc2C(F)(F)F)cc1
Reaction #77834
benzamide
DOI: 10.6084/m9.figshare.5104873.v1
NS(=O)(=O)c1ccc(C(=O)N[C@@H]2CCCC[C@@H]2NC(=O)CNS(=O)(=O)c2cccc(Cl)c2)cc1
Reaction #77835
benzamide
Ausbeute 29.4%DOI: 10.6084/m9.figshare.5104873.v1
CCNC(=O)Nc1ccc(C(F)(F)F)cc1C(=O)NCC(=O)N[C@@H]1CCCC[C@@H]1NC(=O)c1ccc(SC)cc1
Reaction #77837
benzamide
Ausbeute 17.5%DOI: 10.6084/m9.figshare.5104873.v1
NC1CCCCC1N1C[C@H](CCCB(O)O)[C@](N)(C(=O)O)C1
Reaction #89665
(3R,4S)-3-amino-1-(2-aminocyclohexyl)-4-(3-boronopropyl)pyrrolidine-3-carboxylic acid
Ausbeute 99.6%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)[C@H]1CCCC[C@@H]1Nc1nc(-c2c[nH]c3ncc(Cl)cc23)ncc1F
Reaction #162114
desired product
DOI: 10.6084/m9.figshare.5104873.v1
COCCNC(=O)c1nc(N[C@H]2CCCC[C@H]2NC(=O)OC(C)(C)C)c2cc(C)ccc2n1
Reaction #162706
desired compound
DOI: 10.6084/m9.figshare.5104873.v1
COCCNC(=O)c1nc(N[C@H]2CCCC[C@H]2N)c2cc(C)ccc2n1
Reaction #162707
desired compound
Ausbeute 92.0%DOI: 10.6084/m9.figshare.5104873.v1
COCCNC(=O)c1nc(N[C@H]2CCCC[C@H]2NC(C)=N)c2cc(C)ccc2n1
Reaction #162708
desired compound
Ausbeute 77.9%DOI: 10.6084/m9.figshare.5104873.v1
COCCNC(=O)c1nc(N[C@H]2CCCC[C@H]2NC#N)c2cc(C)ccc2n1
Reaction #162710
desired compound
Ausbeute 55.5%DOI: 10.6084/m9.figshare.5104873.v1
Cn1ccc2c(Nc3cc(N[C@@H]4CCCC[C@@H]4NC(=O)OC(C)(C)C)ccc3C#N)cccc21
Reaction #171975
tert-butyl (1S,2R)-2-(4-cyano-3-(1-methyl-1H-indol-4-ylamino)phenylamino)cyclohexylcarbamate
Ausbeute 39.5%DOI: 10.6084/m9.figshare.5104873.v1
Cn1ccc2c(Nc3cc(N[C@@H]4CCCC[C@@H]4N)ccc3C(N)=O)cccc21
Reaction #171976
titled compound
Ausbeute 13.9%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)NC1CCCCC1Nc1nc(Nc2ccc3c(c2)CCN(CC(O)C(F)(F)F)CC3)ncc1Cl
Reaction #174602
DOI: 10.1039/C8SC04228D
CCN1CCCOc2cc(Nc3ncc(Cl)c(NC4CCCCC4NS(C)(=O)=O)n3)c(F)cc21
Reaction #175234
DOI: 10.1039/C8SC04228D
COc1cc2c(cc1Nc1ncc(Cl)c(NC3CCCCC3NS(C)(=O)=O)n1)CCN(CCO)CC2
Reaction #175730
DOI: 10.1039/C8SC04228D
COc1cc2c(cc1Nc1ncc(Cl)c(NC3CCCCC3NS(C)(=O)=O)n1)CCNC(=O)C2
Reaction #176171
DOI: 10.1039/C8SC04228D
COCC(COC)N1CCc2cc(Nc3ncc(Cl)c(NC4CCCCC4NS(C)(=O)=O)n3)c(OC)cc2CC1
Reaction #178642
DOI: 10.1039/C8SC04228D
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