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761828

Cc1csc(NCc2ccccc2)n1
Reaction #715
Ausbeute 0.0%
Cc1cccc2sc(Cl)nc12
Reaction #9662
2-chloro-4-methyl-1,3-benzothiazole
Ausbeute 71.0%DOI: 10.6084/m9.figshare.5104873.v1
Fc1cc(F)c2nc(Cl)sc2c1
Reaction #9663
2-chloro-4,6-difluoro-1,3-benzothiazole
Ausbeute 99.0%DOI: 10.6084/m9.figshare.5104873.v1
FC(F)(F)Oc1ccc2nc(Cl)sc2c1
Reaction #9664
desired compound
DOI: 10.6084/m9.figshare.5104873.v1
Fc1cc(F)c2sc(Cl)nc2c1
Reaction #9667
2-chloro-5,7-difluoro-1,3-benzothiazole
Ausbeute 48.0%DOI: 10.6084/m9.figshare.5104873.v1
FC(F)(F)c1ccc2sc(Cl)nc2c1
Reaction #9671
2-chloro-5-(trifluoromethyl)benzothiazole
Ausbeute 94.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cccc2sc(Nc3ccc(Br)cc3F)nc12
Reaction #9681
N-(4-bromo-2-fluorophenyl)-4-methyl-1,3-benzothiazol-2-amine
Ausbeute 89.4%DOI: 10.6084/m9.figshare.5104873.v1
Fc1ccc2nc(Nc3ccc(Br)cc3F)sc2c1
Reaction #9682
desired product
Ausbeute 78.0%DOI: 10.6084/m9.figshare.5104873.v1
Fc1cc(I)ccc1Nc1nc2ccc(Cl)cc2s1
Reaction #9683
desired product
Ausbeute 38.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(CC(CCc1ccccc1)C(=O)O)c1ccc(-c2ccc(Nc3nc4ccc(Cl)cc4s3)cc2)cc1
Reaction #9689
desired product
Ausbeute 25.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCC(CC(=O)c1ccc(-c2ccc(Nc3nc4ccc(Cl)cc4s3)cc2)cc1)C(=O)O
Reaction #9690
desired product
Ausbeute 18.0%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)CCC(CC(=O)c1ccc(-c2ccc(Nc3nc4ccc(Cl)cc4s3)cc2)cc1)C(=O)O
Reaction #9692
desired product
Ausbeute 16.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)[C@@H]1CC[C@H]1C(=O)c1ccc(-c2ccc(Nc3nc4ccc(Cl)cc4s3)cc2)cc1
Reaction #9707
trans-2-({4′-[(6-chloro-1,3-benzothiazol-2-yl) amino]-1,1′-biphenyl-4-yl}carbonyl)cyclobutanecarboxylic acid
Ausbeute 10.8%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)[C@@H]1CCC[C@H]1C(=O)c1ccc(-c2ccc(Nc3nc4c(F)cc(F)cc4s3)cc2)cc1
Reaction #9709
racemic trans-2-({4′-[(4,6-difluoro-1,3-benzothiazol-2-yl)amino]-1,1-biphenyl-4-yl}-carbonyl)cyclopentanecarboxylic acid
Ausbeute 43.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)[C@@H]1CCC[C@H]1C(=O)c1ccc(-c2ccc(Nc3nc4cc(F)cc(F)c4s3)cc2)cc1
Reaction #9713
trans-2-({4′-[(5,7-difluoro-1,3-benzothiazol-2-yl)amino]-1,1′-biphenyl-4-yl}carbonyl)cyclopentanecarboxylic acid
Ausbeute 58.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)[C@@H]1CCCC[C@H]1C(=O)c1ccc(-c2ccc(Nc3nc4ccc(Cl)cc4s3)cc2)cc1
Reaction #9714
trans-2-({4′-[(6-chloro-1,3-benzothiazol-2-yl)amino]-1,1′-biphenyl-4-yl}carbonyl)cyclohexanecarboxylic acid
Ausbeute 15.5%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)[C@H]1CCC[C@@H](C(=O)c2ccc(-c3ccc(Nc4nc5ccc(Cl)cc5s4)cc3)cc2)C1
Reaction #9717
cis-3-[4′-(6-chloro-benzothiazol-2-ylamino)-biphenyl-4-carbonyl]-cyclohexanecarboxylic acid
Ausbeute 23.4%DOI: 10.6084/m9.figshare.5104873.v1
O=C1C2=C(CCCC2)C(=O)N1c1c(F)cc(Cl)c2nc(Cl)sc12
Reaction #50001
N-(2,4-Dichloro-6-fluorobenzothiazol-7-yl)-3,4,5,6-tetrahydrophthalimide
DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1c(F)cc(Cl)c2nc(Cl)sc12
Reaction #50002
2,4-dichloro-6-fluoro-7-nitrobenzothiazole
DOI: 10.6084/m9.figshare.5104873.v1
Nc1c(F)cc(Cl)c2nc(Cl)sc12
Reaction #50003
7-amino-2,4-dichloro-6-fluorobenzothiazole
DOI: 10.6084/m9.figshare.5104873.v1
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