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1190381

Cc1cc(NC2=NN(c3ccccc3)CC2)cc(C)c1O
Reaction #50552
4-(4,5-dihydro-1-phenyl-1H-pyrazol-3-yl)amino-2,6-dimethylphenol
Выход 46.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)Oc1c(C)cc(NC2=NN(c3ccccc3)CC2)cc1C
Reaction #50554
title product
Выход 46.7%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccn(-c2ccccc2)n1
Reaction #54549
1-phenyl-3-aminopyrazole
DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccn(-c2ccccc2)n1
Reaction #54550
1-phenyl-3-aminopyrazole
Выход 79.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccn(-c2ccccc2)n1
Reaction #54551
1-phenyl-3-aminopyrazole
Выход 50.7%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccn(-c2ccccc2)n1
Reaction #54552
1-phenyl-3-aminopyrazole
Выход 30.4%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccn(-c2ccc(Br)cc2)n1
Reaction #54553
1-(p-bromophenyl)-3-aminopyrazole
Выход 50.5%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccn(-c2cccc(Cl)c2)n1
Reaction #54554
1-(m-chlorophenyl)-3-aminopyrazole
Выход 72.9%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccn(-c2ccc(Cl)cc2)n1
Reaction #54555
1-(p-chlorophenyl)-3-amino-pyrazole
Выход 51.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)NC1=NN(c2c(Cl)cc(Cl)cc2Cl)C(=O)C1
Reaction #95442
3-acetamido-1-(2,4,6-trichlorophenyl)-2-pyrazolin-5-one
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)NC1=NN(c2c(Cl)cc(Cl)cc2Cl)C(=O)C1
Reaction #95443
3-acetamido-1-(2,4,6-trichlorophenyl)-2-pyrazolin-5-one
Выход 48.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1c(Cl)cc(Cl)cc1Cl
Reaction #95444
2,4,6-trichloroaniline
Выход 57.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1CC(Nc2ccc([N+](=O)[O-])cc2)=NN1c1c(Cl)cc(Cl)cc1Cl
Reaction #95445
3-(p-nitroanilino)-1-(2,4,6-trichlorophenyl)-2-pyrazolin-5-one
DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccn(-c2ccccc2)n1
Reaction #170669
titled compound
Выход 24.7%DOI: 10.6084/m9.figshare.5104873.v1
NC1=NN(c2ccc(F)cc2)C(c2cccc(OC(F)(F)F)c2)C1
Reaction #170675
titled compound
DOI: 10.6084/m9.figshare.5104873.v1
Nc1cc(-c2cccc(OC(F)(F)F)c2)n(-c2ccc(F)cc2)n1
Reaction #170676
titled compound
Выход 50.8%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #170696
crude product
DOI: 10.6084/m9.figshare.5104873.v1
CCCc1cccc(-c2cc(N)nn2-c2ccccc2)c1
Reaction #170697
titled compound
Выход 47.0%DOI: 10.6084/m9.figshare.5104873.v1
CCN(CC)CCOc1ccc(N(C(=O)Nc2ccccc2)C2=NN(c3ccccc3)CC2)cc1
Reaction #185801
DOI: 10.1039/C8SC04228D
O=C(NC1=NN(c2cccc(C(=O)O)c2)CC1)Nc1ccccc1
Reaction #188302
DOI: 10.1039/C8SC04228D
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