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O=C1Cc2ccccc2N1

O=C1Cc2ccc(C(=O)c3ccccc3)cc2N1
Reaction #4570
6-benzoyloxindole
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)c1cccc2c1NC(=O)C2
Reaction #4573
7-acetyloxindole
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(N2C(=O)C(=O)c3ccccc32)cc1
Reaction #11295
N-(4-methoxyphenyl)isatin
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2nc3ccccc3c(C(=O)O)c2c1
Reaction #11296
2-Methoxy-acridine-9-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
O=C1Cc2cc(S(=O)(=O)Cl)ccc2N1
Reaction #52587
5-chlorosulfonyl-2-oxindole
Ausbeute 50.0%DOI: 10.6084/m9.figshare.5104873.v1
NS(=O)(=O)c1ccc2c(c1)CC(=O)N2
Reaction #52588
title compound
Ausbeute 20.0%DOI: 10.6084/m9.figshare.5104873.v1
CNS(=O)(=O)c1ccc2c(c1)CC(=O)N2
Reaction #52589
5-methylaminosulfonyl-2-oxindole
Ausbeute 88.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1Cc2cc(S(=O)(=O)Nc3ccc(C(F)(F)F)cc3)ccc2N1
Reaction #52590
5-(4-trifluoromethylphenyl-aminosulfonyl)-2-oxindole
Ausbeute 37.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C1Cc2cc(S(=O)(=O)N3CCOCC3)ccc2N1
Reaction #52591
5-(morpholinosulfonyl)-2-oxindole
Ausbeute 74.9%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(C=C2C(=O)Nc3ccc(S(N)(=O)=O)cc32)[nH]c2ccccc12
Reaction #52756
3-(3-methyl-1H-indol-2-ylmethylene)-2-oxo-2,3-dihydro-1H-indole-5-sulfonic acid amide
Ausbeute 71.0%DOI: 10.6084/m9.figshare.5104873.v1
CNS(=O)(=O)c1ccc2c(c1)CC(=O)N2
Reaction #52757
5-methylaminosulfonyl-2-oxindole
Ausbeute 88.0%DOI: 10.6084/m9.figshare.5104873.v1
NS(=O)(=O)c1ccc2c(c1)C(=Cc1cc3ccccc3[nH]1)C(=O)N2
Reaction #52764
3-(1H-indol-2-ylmethylene)-2-oxo-2,3-dihydro-1H-indole-5-sulfonic acid amide
Ausbeute 83.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1Cc2cc(S(=O)(=O)Cl)ccc2N1
Reaction #52799
5-chlorosulfonyl-2-oxindole
Ausbeute 50.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)NS(=O)(=O)c1ccc2c(c1)CC(=O)N2
Reaction #52800
5-isopropylaminosulfonyl-2-oxindole
Ausbeute 45.5%DOI: 10.6084/m9.figshare.5104873.v1
O=C1Nc2ccccc2/C1=C(/Nc1ccc(S(=O)(=O)N2CCCC2)cc1)c1ccccc1
Reaction #53228
(Z)-3-{1-[4-(pyrrolidin-1-ylsulphonyl)-phenylamino]-1-phenyl-methylidene}-2-indolinone
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccccc1C1(O)C(=O)Nc2ccc(OC(F)(F)F)cc21
Reaction #59630
expected product
Ausbeute 76.3%DOI: 10.6084/m9.figshare.5104873.v1
NS(=O)(=O)c1ccc2c(c1)C(=Cc1cc3cc(OCCN4CCCC4)ccc3[nH]1)C(=O)N2
Reaction #77366
title compound
Ausbeute 80.0%DOI: 10.6084/m9.figshare.5104873.v1
NS(=O)(=O)c1ccc2c(c1)C(=Cc1cc3cc(OCCN4CCOCC4)ccc3[nH]1)C(=O)N2
Reaction #77367
title compound
Ausbeute 73.7%DOI: 10.6084/m9.figshare.5104873.v1
CNS(=O)(=O)c1ccc2c(c1)C(=Cc1cc3cc(OCCN4CCCC4)ccc3[nH]1)C(=O)N2
Reaction #77368
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C1Nc2ccc(S(=O)(=O)Nc3ccccc3)cc2C1=Cc1cc2cc(OCCN3CCCC3)ccc2[nH]1
Reaction #77370
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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