6-methyl-3-chloropyridazine

CCOC(=O)C1CCN(c2ccc(C)nn2)CC1
Reaction #5042
3-(4-carboethoxy-1-piperidinyl)-6-methylpyridazine
Rendimiento 44.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
Cc1ccc(-n2nccn2)c(C(=O)N2CCC[C@@H](C)[C@H]2CNc2ccc(C)nn2)c1
Reaction #89346
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
Cc1ccc(-n2cc(C#Cc3cccc(Cl)c3)nc2C)nn1
Reaction #176698
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1ccc(-c2ccc(C(C)N3CCC(CC(C)(C)O)(c4ccccc4)OC3=O)cc2)nn1
Reaction #180129
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1ccc(C#Cc2cccnc2)nn1
Reaction #180568
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cc1ccc(-c2ccc(C(C)N3CCC(CC(C)(C)O)(c4ccccc4)OC3=O)cc2)nn1
Reaction #235272
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=C(O)c1ccc(Cl)nn1
Reaction #253826
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cc1ccc(NCCN)nn1
Reaction #269478
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Cc1ccc(OCc2c(-c3ccccc3)noc2C)nn1
Reaction #277776
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Cc1ccc(NCc2ccccc2)nn1
Reaction #278997
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COC(=O)C1CN(c2ccc(C)nn2)CC1c1ccc(Cl)cc1
Reaction #280085
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COC(=O)C1CN(c2ccc(C)nn2)CC1c1ccc(Cl)cc1
Reaction #283917
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
ClCc1ccc(Cl)nn1
Reaction #302214
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Cc1ccc(NN)nn1
Reaction #387188
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CCOC(=O)C1CCN(c2ccc(C)nn2)CC1
Reaction #392481
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
Cc1ccc(-c2ccc(C(C)N3CCC(CCCO)(c4ccc(F)cc4)OC3=O)cc2)nn1
Reaction #404712
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
Cc1ccc(Nc2ccc3c(c2)N(c2nc4c(s2)C(=O)CC(C)(C)C4)CCO3)nn1
Reaction #505124
title compound
Rendimiento 26.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_01
Cc1ccc(Oc2cccc3c2[C@H]2CCCN(C(=O)OC(C)(C)C)[C@H]2CC3)nn1
Reaction #542527
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_07
Cc1ccc(N2CCC(CCO)CC2)nn1
Reaction #571681
1-(6-methyl-3-pyridazinyl) -4-piperidineethanol
Rendimiento 95.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_07
CCOC(=O)c1ccc(OCCC2CCN(c3ccc(C)nn3)CC2)cc1
Reaction #571692
ethyl 4-[2-[1-(6-methyl-3-pyridazinyl)-4-piperidinyl]ethoxy ]benzoate
Rendimiento 56.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_07
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