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CCl

CCc1cccc(C)c1S(=O)(=O)c1nn(C(=O)N(CC)CC)c(SC)c1Cl
Reaction #49888
title compound
Ausbeute 35.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(-c2nc3sc4ccccc4n3c2CC(=O)N(C)C)c(C)s1
Reaction #65188
N,N-Dimethyl-2-(2,5-dimethylthien-3-yl)imidazo[2,1-b]-benzothiazole-3-acetamide
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(-c2nc3sc4ccc(Cl)cc4n3c2C(Cl)C(=O)N(C)C)c(C)s1.Cl
Reaction #65191
α,6-dichloro-N,N-dimethyl-2-(2,5-dimethylthien-3-yl)imidazo[2,1-b]benzothiazole-3-acetamide hydrochloride
Ausbeute 205.2%DOI: 10.6084/m9.figshare.5104873.v1
Nc1n[nH]cc1-c1cc(C(F)(F)F)ccc1Oc1cc(F)c(S(=O)(=O)Nc2nncs2)cc1Cl
Reaction #74542
aminopyrazole
DOI: 10.6084/m9.figshare.5104873.v1
O=c1[nH]c2cc(C(F)(F)F)ccc2n1CCCCl
Reaction #75122
1-(3-chloropropyl)-1,3-dihydro-5-(trifluoromethyl)-2H-benzimidazol-2-one
Ausbeute 56.0%DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)n1c(=O)n(CC(C)CCl)c2ccccc21
Reaction #75146
1-(3-chloro-2-methylpropyl)-1,3-dihydro-3-(1-methylethenyl)-2H-benzimidazol-2-one
Ausbeute 90.6%DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)n1c(=O)n(CCCN2CCC(n3c(=O)[nH]c4ccccc43)CC2)c2ccc(C)cc21
Reaction #75181
1-{3-[4-(2,3-dihydro-2-oxo-1H-benzimidazol-1-yl)-1-piperidinyl]propyl}-1,3-dihydro-5-methyl-3-(1-methylethenyl)-2H-benzimidazol-2-one
Ausbeute 67.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CNc2ncnc3c(N4CCOCC4)nc(Cl)nc23)cc1
Reaction #81434
2-chloro-8-(4-methoxy-benzylamino)-4-morpholino-pyrimido[5,4-d]pyrimidine
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1c(Cl)ccc(CNC(=O)C(C)(C)C)c1F
Reaction #87617
product
Ausbeute 63.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1cnn2ccc(N3CCC[C@@H]3c3cc(F)cc(Cl)c3)nc12)N1CC(O)C1
Reaction #92273
final product
Ausbeute 74.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(O)CN(C(=O)Nc2cnn3ccc(N4CCC[C@@H]4c4cc(F)ccc4Cl)nc23)C1
Reaction #92281
final product
Ausbeute 71.5%DOI: 10.6084/m9.figshare.5104873.v1
CON=C(c1cccc(F)c1)C1CN(c2ncc(Cl)cc2C(=O)NC2(c3ccc(C(=O)O)cc3)CC2)C1
Reaction #159731
title compound ( E26 )
Ausbeute 22.9%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
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
CC(C)S(=O)(=O)N1CC[C@H](Nc2nc(-c3c[nH]c4ncc(Cl)cc34)ncc2F)C1
Reaction #162070
400
Ausbeute 39.0%DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(C1CC1)N1CC[C@H](Nc2nc(-c3c[nH]c4ncc(Cl)cc34)ncc2F)C1
Reaction #162071
401
Ausbeute 37.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCS(=O)(=O)N1CC[C@H](Nc2nc(-c3c[nH]c4ncc(Cl)cc34)ncc2F)C1
Reaction #162072
402
Ausbeute 45.0%DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(C1CCCC1)N1CC[C@H](Nc2nc(-c3c[nH]c4ncc(Cl)cc34)ncc2F)C1
Reaction #162073
403
Ausbeute 20.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCS(=O)(=O)N1CC[C@H](Nc2nc(-c3c[nH]c4ncc(Cl)cc34)ncc2F)C1
Reaction #162074
410
Ausbeute 36.0%DOI: 10.6084/m9.figshare.5104873.v1
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