Recherche de Sous-structure

CNCC=C

C[N+]1(CC2=C(C(=O)[O-])N3C(=O)[C@@H](NC(=O)C(=NOCC(=O)O)c4nsc(N)n4)[C@H]3SC2)CCNCC1

7β-[2-(5-amino-1,2,4-thiadiazol-3-yl)-2-carboxymethoxyiminoacetamido]-3-(1-methyl-1-piperazinio)methyl-3-cephem-4-carboxylate

Rendement 33.0%DOI: 10.6084/m9.figshare.5104873.v1

Reaction #40778

colorless oil

Rendement 98.9%DOI: 10.6084/m9.figshare.5104873.v1

COc1ccc(CN2CC(c3cccc(F)c3F)=CC[C@@H](NC(=O)OCc3ccccc3)C2=O)c(OC)c1

Reaction #42664

title compound

Rendement 57.5%DOI: 10.6084/m9.figshare.5104873.v1

O=C(N[C@@H]1CC=C(c2cccc(F)c2F)CNC1=O)OCc1ccccc1

Reaction #42665

title compound

Rendement 66.4%DOI: 10.6084/m9.figshare.5104873.v1

Reaction #47744

product

Rendement 46.0%DOI: 10.6084/m9.figshare.5104873.v1

Reaction #48408

title compound

Rendement 57.5%DOI: 10.6084/m9.figshare.5104873.v1

Reaction #48409

title compound

Rendement 66.4%DOI: 10.6084/m9.figshare.5104873.v1

$CCCN(CCC)C(=O)/C=C(\C)C(=O)N[C@@H](Cc1cc(F)cc(F)c1)[C@H](O)[C@H]1CO[C@@H](COC2CCCCC2)CN1C(=O)OC(C)(C)C$

Reaction #48661

title compound

Rendement 45.2%DOI: 10.6084/m9.figshare.5104873.v1

$CCCN(CCC)C(=O)/C=C(\C)C(=O)N[C@@H](Cc1cc(F)cc(F)c1)[C@H](O)[C@H]1CO[C@@H](OCC2CCCCC2)CN1C(=O)O.Cl$

Reaction #48756

title compound

Rendement 97.3%DOI: 10.6084/m9.figshare.5104873.v1

CC1=C(C(=O)OCc2ccccc2)C(c2cccc(Cl)c2)N(C(=O)NCCC(c2ccccc2)c2ccccc2)C(=O)N1

Reaction #52891

title compound

DOI: 10.6084/m9.figshare.5104873.v1

$CN(C(=O)CN1CCN(Cc2ccccc2)CC1)c1ccc(N/C(=C2\C(=O)Nc3ccccc32)c2ccccc2)cc1$

Reaction #53055

(Z)-3-{1-[4-(N-(4-benzylpiperazinomethylcarbonyl)-N-methyl-amino)-phenylamino]-1-phenyl-methylidene}-2-indolinone

DOI: 10.6084/m9.figshare.5104873.v1

$CN(C(=O)CN1CCNCC1)c1ccc(N/C(=C2\C(=O)Nc3ccccc32)c2ccccc2)cc1.Cl.Cl$

Reaction #53056

(Z)-3-{1-[4-(N-piperazinomethylcarbonyl-N-methyl-amino)-phenylamino]-1-phenyl-methylidene}-2-indolinone-dihydrochloride

DOI: 10.6084/m9.figshare.5104873.v1

$N#Cc1ccc(N/C(=C2\C(=O)Nc3ccc([N+](=O)[O-])cc32)c2ccccc2)cc1$

Reaction #53081

(Z)-3-[1-(4-cyanophenylamino)-1-phenyl-methylidene]-5-nitro-2-indolinone

DOI: 10.6084/m9.figshare.5104873.v1

$N#Cc1cccc(N/C(=C2\C(=O)Nc3ccc([N+](=O)[O-])cc32)c2ccccc2)c1$

Reaction #53082

(Z)-3-[1-(3-cyanophenylamino)-1-phenyl-methylidene]-5-nitro-2-indolinone

DOI: 10.6084/m9.figshare.5104873.v1

$O=C(CN1CCOCC1)Nc1ccc(N/C(=C2\C(=O)Nc3ccc([N+](=O)[O-])cc32)c2ccccc2)cc1$

Reaction #53092

(Z)-3-[1-(4-morpholinomethylcarbonylamino-phenylamino)-1-phenyl-methylidene]-5-nitro-2-indolinone

DOI: 10.6084/m9.figshare.5104873.v1

$CN1CCN(CC(=O)Nc2ccc(N/C(=C3\C(=O)Nc4ccc([N+](=O)[O-])cc43)c3ccccc3)cc2)CC1$

Reaction #53093

(Z)-3-{1-[4-(4-methylpiperazinomethylcarbonylamino)-phenylami-no]-1-phenyl-methylidene}-5-nitro-2-indolinone

DOI: 10.6084/m9.figshare.5104873.v1

$CN(C(=O)CN1CCOCC1)c1ccc(N/C(=C2\C(=O)Nc3ccc([N+](=O)[O-])cc32)c2ccccc2)cc1$

Reaction #53095

(Z)-3-{1-[4-(N-morpholinomethylcarbonyl-N-methyl-amino)-phenylamino]-1-phenyl-methylidene}-5-nitro-2-indolinone

DOI: 10.6084/m9.figshare.5104873.v1

$CN1CCN(CC(=O)N(C)c2ccc(N/C(=C3\C(=O)Nc4ccc([N+](=O)[O-])cc43)c3ccccc3)cc2)CC1$

Reaction #53096

(Z)-3-{-[4-(N—(N-methylpiperazinomethylcarbonyl)-N-methyl-amino)-phenylamino]-1-phenyl-methylidene}-5-nitro-2-indolinone

DOI: 10.6084/m9.figshare.5104873.v1

$CN(C(=O)CN1CCNCC1)c1ccc(N/C(=C2\C(=O)Nc3ccc([N+](=O)[O-])cc32)c2ccccc2)cc1.Cl.Cl$

Reaction #53098

(Z)-3-{1-[4-(N-piperazinomethylcarbonyl-N-methyl-amino)phenylamino]-1-phenyl-methylidene}-5-nitro-2-indolinone-dihydrochloride

DOI: 10.6084/m9.figshare.5104873.v1

$Cl.NCC(=O)NCc1ccc(N/C(=C2\C(=O)Nc3ccc([N+](=O)[O-])cc32)c2ccccc2)cc1$

Reaction #53108

(Z)-3-[1-(4-aminomethylcarbonylaminomethyl-phenylamino]-1-phenyl-methylidene}-5-nitro-2-indolinone-hydrochloride

DOI: 10.6084/m9.figshare.5104873.v1

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