Substructure Search

C1COCCC1NN.Cl

Cl.NNC1CCOCC1
Reaction #41160
(tetrahydro-pyran-4-yl)-hydrazine hydrochloride
Yield 60.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cnn(C2CCOCC2)c1N
Reaction #41161
5-amino-1-(tetrahydro-pyran-4-yl)-1H-pyrazole-4-carboxylic acid ethyl ester
Yield 92.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)Nc1cc(C)c(Br)cc1-c1ccnn1C1CCOCC1
Reaction #156288
N-{4-bromo-5-methyl-2-[1-(tetrahydro-2H-pyran-4-yl)-1H-pyrazol-5-yl]phenyl}acetamide
Yield 56.7%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1cc(C(F)(F)F)c(Br)cc1-c1ccnn1C1CCOCC1)C(F)(F)F
Reaction #156297
N-{4-bromo-2-[1-(tetrahydro-2H-pyran-4-yl)-1H-pyrazol-5-yl]-5-(trifluoromethyl)phenyl}-2,2,2-trifluoroacetamide
Yield 42.1%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #687273
mixture
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #837100
mixture
DOI: 10.6084/m9.figshare.5104873.v1
CC1CC(N)CCO1.Cl
Reaction #989758
4-amino-2-methyltetrahydropyran hydrochloride
Yield 64.3%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H]1C[C@@H](S(=O)(=O)c2ccccc2C(F)(F)F)CN1c1cc(C)nn1C1CCOCC1
Reaction #1784774
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H]1C[C@@H](S(=O)(=O)c2ccc(F)cc2C(F)(F)F)CN1c1cc(C)nn1C1CCOCC1
Reaction #1784854
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H]1C[C@@H](S(=O)(=O)c2ccc(F)cc2Cl)CN1c1cc(C)nn1C1CCOCC1
Reaction #1784923
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H]1C[C@@H](S(=O)(=O)c2ccccc2Cl)CN1c1cc(C)nn1C1CCOCC1
Reaction #1784953
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Clc1ccc(-c2nn(C3CCOCC3)c3c2CCNCC3)cc1
Reaction #2193582
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cl.Cl.NNC1CCOCC1
Reaction #2293178
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1nccc(I)c1C(=O)NNC1CCOCC1
Reaction #2293179
title compound
Yield 81.2%DOI: 10.6084/m9.figshare.5104873.v1