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18884

Clc1nn2c(-c3ccccc3)nnc2cc1C1CCC1
Reaction #11322
title compound
Ausbeute 34.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)N(C(=O)c1ccccc1)N(Cc1ccccc1)C(=O)c1ccccc1
Reaction #49906
N-benzyl-N'-t-butyl-N,N'-dibenzoylhydrazine
DOI: 10.6084/m9.figshare.5104873.v1
CC(=NNC(=O)c1ccccc1)c1ccccc1
Reaction #50376
Acetophenone N-Benzoylhydrazone
DOI: 10.6084/m9.figshare.5104873.v1
Cn1c(CCc2ccc(C(=N)NC(=O)c3ccccc3)cc2)nc2cc(C(=O)NN3CCC(NC(=O)c4ccccc4)CC3)ccc21
Reaction #52191
2-[2-(4-Benzoylamidinophenyl)-ethyl]-1-methyl-benzimidazole-5-yl-carboxylic acid-(4-benzamidopiperidinyl)-amide
DOI: 10.6084/m9.figshare.5104873.v1
CCC(=N)N(N)C(=O)c1ccc(OC)cc1
Reaction #58080
4-methoxy-benzoic acid-(1-imino-propyl)-hydrazide
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cccc(C(=O)NNC(=O)OCc2ccccc2)c1
Reaction #58081
methyl 3-[N′-benzyloxycarbonyl-hydrazinocarbonyl)-benzoate
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cccc(C(=O)NN)c1
Reaction #58082
methyl 3-hydrazinocarbonyl-benzoate
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C(=O)NNC(C)=N)cc1
Reaction #58090
4-methoxy-benzoic acid N′-(1-imino-ethyl)-hydrazide
DOI: 10.6084/m9.figshare.5104873.v1
CN=C(CCCC1OCCCO1)NNC(=O)c1ccc2nc(C)ccc2c1
Reaction #61503
desired compound
Ausbeute 83.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc2cc(-c3nnc(CCCC4OCCCO4)n3C)ccc2n1
Reaction #61504
title compound
Ausbeute 10.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(Nc1ncnc2cc(C(=O)N3CCCN3)c(Cl)cc12)c1nc2cc(Cl)ccc2[nH]1
Reaction #62492
6-chloro-4-[1-(5-chloro-1H-benzimidazol-2-yl)-ethylamino]-7-(pyrazolidin-1-yl-carbonyl)-quinazoline
DOI: 10.6084/m9.figshare.5104873.v1
CCc1ccc(C(=O)NN(C(=O)c2cc(C)cc(C)c2)C(C)(C)C)c(F)c1
Reaction #67907
3,5-Dimethyl-benzoic acid N-tert-butyl-N′-(4-ethyl-2-fluoro-benzoyl)-hydrazide
DOI: 10.6084/m9.figshare.5104873.v1
CCc1c(C(=O)NN)ccc2c1OCCO2
Reaction #67930
5-ethyl-2,3-dihydro-benzo[1,4]dioxine-6-carboxylic acid hydrazide
Ausbeute 129.9%DOI: 10.6084/m9.figshare.5104873.v1
c1ccc(-c2ncc(-c3nnc(-c4ccccc4)[nH]3)cn2)cc1
Reaction #70585
title compound
Ausbeute 6.1%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #72497
solid
Ausbeute 31.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N1CCC(=NNC(=O)c2ccccc2)CC1
Reaction #72924
title compound
Ausbeute 83.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N1CCC(N(NC(=O)OC(C)(C)C)C(=O)OC(C)(C)C)CC1
Reaction #72926
title compound
Ausbeute 89.5%DOI: 10.6084/m9.figshare.5104873.v1
Cc1nc(NC(=O)c2ccccc2)sc1C(=O)NNC(=O)c1ccccc1
Reaction #73655
title compound
Ausbeute 14.0%DOI: 10.6084/m9.figshare.5104873.v1
N#CC1c2ccccc2C(Nc2ccc(Cl)cc2)=NN1C(=O)c1ccccc1
Reaction #78190
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Nc1cc(Br)ccc1C(=O)NNc1ccccc1
Reaction #155849
2-amino-4-bromo-N′-phenylbenzohydrazide
DOI: 10.6084/m9.figshare.5104873.v1
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