Recherche de Sous-structure

10930

OC1(c2cccc3c2OCCO3)CCN(Cc2ccccc2)CC1
Reaction #5067
1-Benzyl-4-hydroxy-4-(1,4-benzodioxan-5-yl)piperidine
DOI: 10.6084/m9.figshare.5104873.v1
OC1(c2nccn2CCc2ccccc2)CCN(Cc2ccccc2)CC1
Reaction #7502
4-[1-(2-phenylethyl)-1H-imidazol-2-yl]-1-(phenylmethyl)-4-piperidinol
Rendement 75.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(CN2C3CCC2CC(=O)C3)cc1
Reaction #44775
methyl 4-[(3-oxo-8-azabicyclo[3.2.1]oct-8-yl)methyl]-benzoate
Rendement 75.5%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccncc1NC1CCN(Cc2ccccc2)CC1
Reaction #48353
title compound
Rendement 98.2%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cc2c(nc1N)CCN(Cc1ccccc1)C2
Reaction #49975
2-amino-6-benzyl-5,6,7,8-tetrahydro-1,6-naphthyridine-3-carbonitrile
Rendement 49.5%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cc2c(nc1N)CCN(Cc1ccccc1)C2
Reaction #49978
2-amino-6-benzyl-5,6,7,8-tetrahydro-1,6-naphthyridine-3-carbonitrile
Rendement 49.5%DOI: 10.6084/m9.figshare.5104873.v1
O=C1CC2CCC(C1)N2Cc1ccccc1
Reaction #52207
title compound
Rendement 46.6%DOI: 10.6084/m9.figshare.5104873.v1
CON=C1CCN(Cc2ccccc2)CC1
Reaction #54244
1-benzyl-4-methoxyiminopiperidine
DOI: 10.6084/m9.figshare.5104873.v1
NCCCNC1CCN(Cc2ccccc2)CC1
Reaction #54245
4-(3-aminopropylamino)-1-benzylpiperidine
DOI: 10.6084/m9.figshare.5104873.v1
c1ccc(CN2CCC(NCCNc3ccccc3)CC2)cc1
Reaction #54248
1-benzyl-4-(2-phenylaminoethylamino)-piperidine
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #55008
27
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #56402
27
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #56795
N-benzyltropanone
DOI: 10.6084/m9.figshare.5104873.v1
O=C1CC2CCC(C1)N2Cc1ccccc1
Reaction #56800
title intermediate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)NC1CCN(C(=O)c2ccc(Nc3nccc(-c4ccc(Cl)cc4)n3)cc2)CC1.Cl
Reaction #61733
4-{[4-(4-chlorophenyl)pyrimidin-2-yl]amino}phenyl 4-[(methylethyl)amino]piperidyl ketone hydrochloride
Rendement 62.9%DOI: 10.6084/m9.figshare.5104873.v1
c1ccc(CN2C3CCC2CC2(CO2)C3)cc1
Reaction #68978
8-Benzyl-spiro[8-azabicyclo[3.2.1]octane-3,2′-oxirane]
DOI: 10.6084/m9.figshare.5104873.v1
N#CC1(N2CCN(C3CC3)CC2)CCN(Cc2ccccc2)CC1
Reaction #74272
desired product
Rendement 53.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(N(C)C(=O)CC2(O)CCN(Cc3ccccc3)CC2)cc1
Reaction #78236
titled compound
Rendement 69.7%DOI: 10.6084/m9.figshare.5104873.v1
CCOc1ccc(N(C)C(=O)CC2(O)CCN(Cc3ccccc3)CC2)cc1
Reaction #78237
titled compound
Rendement 56.3%DOI: 10.6084/m9.figshare.5104873.v1
CCCCOc1ccc(N(C)C(=O)CC2(O)CCN(Cc3ccccc3)CC2)cc1
Reaction #78238
titled compound
Rendement 52.3%DOI: 10.6084/m9.figshare.5104873.v1
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