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CC(C)NN.Cl

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Reaction #2191
powder
Выход 91.5%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1c(C)nn(C2CCCCC2)c1C
Reaction #8162
1-cyclohexyl-3,5-dimethyl-1H-pyrazole-4-carboxylic acid ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cnn(C2CCCCC2)c1N
Reaction #41156
5-amino-1-cyclohexyl-1H-pyrazole-4-carboxylic acid ethyl ester
Выход 92.9%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cnn(C2CCCCC2)c1C(F)(F)F
Reaction #41171
1-cyclohexyl-5-trifluoromethyl-1H-pyrazole-4-carboxylic acid ethyl ester
Выход 58.5%DOI: 10.6084/m9.figshare.5104873.v1
Clc1ccccc1C1CC1C1CC1
Reaction #45299
2-(2-chlorophenyl)bicyclopropyl
Выход 89.8%DOI: 10.6084/m9.figshare.5104873.v1
CN=C(NS(=O)(=O)c1ccc(Cl)cc1)C1=NN(c2ccc(Cl)cc2)C(c2ccccc2)C1
Reaction #48039
N-[(4-chlorophenyl)sulfonyl]-N′-methyl-1-(4-chlorophenyl)-5-phenyl-4,5-dihydro-(1H)-pyrazole-3-carboxamidine
Выход 15.0%DOI: 10.6084/m9.figshare.5104873.v1
CN=C(NS(=O)(=O)N1CCCCC1)C1=NN(c2ccc(Cl)cc2)C(c2ccccc2)C1
Reaction #48040
N-[(piperidin-1-yl)sulfonyl]-N′-methyl-1-(4-chlorophenyl)-5-phenyl-4,5-dihydro-(1H)-pyrazole-3-carboxamidine
Выход 49.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)N(NC(=O)c1ccccc1)P(C)(=O)Nc1ccccc1Cl
Reaction #49948
N'-t-butyl-N'-[methyl-(2-chlorophenylamino)phosphinyl]-N-benzoylhydrazine
DOI: 10.6084/m9.figshare.5104873.v1
O=C(CNC(=O)OCc1ccccc1)NCc1nncn1-c1ccc(Cl)cc1C(=O)c1ccccc1
Reaction #54220
5-chloro-2-[3-(N-carbobenzoxyglycyl)aminomethyl-4H-1,2,4-triazol-4-yl]-benzophenone
Выход 35.6%DOI: 10.6084/m9.figshare.5104873.v1
Oc1ccc(F)cc1-c1ccnn1C1CN(C(c2ccccc2)c2ccccc2)C1
Reaction #74631
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Oc1ccc(Cl)cc1-c1ccnn1C1CN(C(c2ccccc2)c2ccccc2)C1
Reaction #74633
title compound
Выход 42.0%DOI: 10.6084/m9.figshare.5104873.v1
Cl.Cl.NNC1CN(C(c2ccccc2)c2ccccc2)C1
Reaction #74634
title compound
Выход 85.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(Cl)nn1-c1cccnc1
Reaction #85360
methyl 3-chloro-1-(pyridin-3-yl)-1H-pyrazole-5-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1CC(Cl)=NN1c1cccnc1
Reaction #85389
desired product
Выход 65.7%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(Cl)nn1-c1cccnc1
Reaction #85390
desired product
Выход 57.4%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(Cl)nn1-c1cccnc1
Reaction #85391
desired product
Выход 36.2%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CC(Cl)=NN1c1cccnc1
Reaction #85398
title compound
Выход 79.7%DOI: 10.6084/m9.figshare.5104873.v1
CN1CC[C@H](NN)C1.Cl.Cl
Reaction #156306
(3S)-3-hydrazino-1-methylpyrrolidine dihydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)CCCCC(=O)N1Nc1nc(-c2c[nH]c3ncc(Cl)cc23)ncc1F
Reaction #162144
(2-(5-chloro-1H-pyrrolo[2,3-b]pyridin-3-yl)-5-fluoropyrimidin-4-ylamino)-7,7-dimethylazepan-2-one
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(N2CCC(N(C)N3C(=O)CN(S(=O)(=O)c4ccc5cc(Cl)ccc5c4)CC3C(=O)O)CC2)ccn1
Reaction #178382
DOI: 10.1039/C8SC04228D
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