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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
Ausbeute 75.0%DOI: 10.6084/m9.figshare.5104873.v1
ON=C1CCN(Cc2ccccc2)C1
Reaction #10443
1-benzylpyrrolidin-3-one oxime
Ausbeute 102.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCCCN(Cc2ccccc2)C1
Reaction #40342
desired title compound
Ausbeute 45.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1CN(Cc2ccccc2)CCCC1Br
Reaction #40343
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccncc1NC1CCN(Cc2ccccc2)CC1
Reaction #48353
title compound
Ausbeute 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
Ausbeute 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
Ausbeute 49.5%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
CCCCCCC(C)(C)c1ccc(C2(O)CCCN(Cc3ccccc3)C2)c(OCc2ccccc2)c1
Reaction #54339
title compound
Ausbeute 67.0%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
N#CC1(N2CCN(C3CC3)CC2)CCN(Cc2ccccc2)CC1
Reaction #74272
desired product
Ausbeute 53.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(CN2CCC(=O)CC2)cc1
Reaction #77721
1-(4-methylbenzyl)-4-piperidinone
Ausbeute 81.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(CN2CCC(N)CC2)cc1
Reaction #77722
amine
Ausbeute 48.9%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(N(C)C(=O)CC2(O)CCN(Cc3ccccc3)CC2)cc1
Reaction #78236
titled compound
Ausbeute 69.7%DOI: 10.6084/m9.figshare.5104873.v1
CCOc1ccc(N(C)C(=O)CC2(O)CCN(Cc3ccccc3)CC2)cc1
Reaction #78237
titled compound
Ausbeute 56.3%DOI: 10.6084/m9.figshare.5104873.v1
CCCCOc1ccc(N(C)C(=O)CC2(O)CCN(Cc3ccccc3)CC2)cc1
Reaction #78238
titled compound
Ausbeute 52.3%DOI: 10.6084/m9.figshare.5104873.v1
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