بحث البنية الفرعية

ClCCN1CCCCC1

Cl.O=C(c1ccc(F)cc1)C1CCN(CCCl)CC1
Reaction #2554
title compound
المردود 96.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccc(F)cc1)C1CCN(CCCl)CC1
Reaction #2555
title compound
المردود 92.3%DOI: 10.6084/m9.figshare.5104873.v1
COCc1ccc(C(=O)N(CCN2CCC(C(=O)c3ccc(F)cc3)CC2)c2ccccc2OC)cc1
Reaction #2564
title compound
المردود 54.7%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccccc1N(CCN1CCC(C(=O)c2ccc(F)cc2)CC1)S(=O)(=O)c1ccc(C)cc1
Reaction #2565
title compound
المردود 91.5%DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccccc1)C1CCN(CCN(C(=O)c2ccc([N+](=O)[O-])cc2)c2cccnc2)CC1
Reaction #2613
title compound
المردود 24.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc(OCCN2CCCCC2)cc1
Reaction #2879
Ethyl 4-(2-Piperidinoethoxy)benzoate
DOI: 10.6084/m9.figshare.5104873.v1
N#CC(CCN1CCCCC1)c1ccccc1Cl
Reaction #3052
(±)-α-(2-chlorophenyl)-1-piperidinebutanenitrile
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #3054
( b )
DOI: 10.6084/m9.figshare.5104873.v1
CCCCC12CCC(=O)C(c3ccc(OCCN4CCCCC4)cc3)=C1c1ccc(OC)cc1C2
Reaction #7936
9a-butyl-7-methoxy-4-{4-[2-(1-piperidinyl)ethoxy]phenyl}-1,2,9,9a-tetrahydro-3H-fluoren-3-one
المردود 96.3%DOI: 10.6084/m9.figshare.5104873.v1
CC1(O)CCN(CCCl)CC1
Reaction #45266
1-(2-chloroethyl)-4-methylpiperidin-4-ol
DOI: 10.6084/m9.figshare.5104873.v1
OC1(C(F)(F)F)CCN(CCCl)CC1
Reaction #45268
1-(2-chloroethyl)-4-(trifluoromethyl)piperidin-4-ol
DOI: 10.6084/m9.figshare.5104873.v1
Cl.Cl.N=C(NOCC(Cl)CN1CCCCC1)c1cccnc1
Reaction #48028
N-[2-chloro-3-(1-piperidinyl)propoxy]-3-pyridine-carboximidamide dihydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
c1cncc(C2=NOCC(CN3CCCCC3)N2)c1
Reaction #48029
5,6-Dihydro-5-(1-piperidinyl)methyl-3-(3-pyridyl)-4H-1,2,4-oxadiazine
DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)Nc1ccc(NS(C)(=O)=O)c(SCCN2CCCCC2)c1.Cl
Reaction #54200
title compound
DOI: 10.6084/m9.figshare.5104873.v1
NC1(C(=O)N2CCCCC2)C=CC=CN1
Reaction #58481
2-aminopyridinoyl-piperidine
DOI: 10.6084/m9.figshare.5104873.v1
CNCCN1CCCCC1
Reaction #62990
N-methyl-N-(2-piperidinoethyl)amine
المردود 73.0%DOI: 10.6084/m9.figshare.5104873.v1
CO[C@@H]1CN(C(=O)CCl)CC[C@@H]1NC(=O)OCc1ccccc1
Reaction #72091
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(CC(=O)N1CC[C@H](NC(=O)OCc2ccccc2)[C@H](OC)C1)C(C)=O
Reaction #72092
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C1CC2(CCCC2)CC(=O)N1CCN1CCN(c2cc(F)ccc2F)CC1
Reaction #77298
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C1CC2(CCCC2)CC(=O)N1CCN1CCN(c2cc(F)c(F)cc2F)CC1
Reaction #77299
title compound
DOI: 10.6084/m9.figshare.5104873.v1
الصفحة 1التالي