Substructure Search

4184

Cl.O=C(c1ccc(F)cc1)C1CCN(CCCl)CC1
Reaction #2554
title compound
Yield 96.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccc(F)cc1)C1CCN(CCCl)CC1
Reaction #2555
title compound
Yield 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
Yield 54.7%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
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
Yield 96.3%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
CNCCN1CCCCC1
Reaction #62990
N-methyl-N-(2-piperidinoethyl)amine
Yield 73.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc(OCCN2CCCCC2)cc1
Reaction #79142
Ethyl 4-(2-Piperidinylethoxy)benzoate
DOI: 10.6084/m9.figshare.5104873.v1
O=C(C(Cl)Cl)N1CCC2(CC1)OCCO2
Reaction #93665
N-dichloroacetylpiperid-4-one ethylene ketal
Yield 49.2%DOI: 10.6084/m9.figshare.5104873.v1
CC1COC2(CCN(C(=O)C(Cl)Cl)CC2)O1
Reaction #93666
N-dichloroacetyl-piperid-4-one propylene ketal
Yield 66.6%DOI: 10.6084/m9.figshare.5104873.v1
CCCC(=O)c1ccc(OCCN2CCCCC2)cc1Cl
Reaction #94889
1-[2-Chloro-4-(2-piperidinoethoxy)phenyl]-1-butanone
DOI: 10.6084/m9.figshare.5104873.v1
Reaction #172842
solid
Yield 83.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc2ncnc(Nc3cccc(Cl)c3F)c2cc1OC1CCN(C(=O)CN2CCOCC2)CC1
Reaction #181567
DOI: 10.1039/C8SC04228D
O=C(CNc1ccc2[nH]c(=O)oc2c1)N1CCC(Oc2ccc(Cl)cc2)CC1
Reaction #186698
DOI: 10.1039/C8SC04228D
O=C(C(Cl)Cl)N1CCC2(CC1)OCCO2
Reaction #198568
DOI: 10.1039/C8SC04228D
COc1cc2ncnc(Nc3cccc(Cl)c3F)c2cc1OC1CCN(C(=O)CN2CCCC2)CC1
Reaction #207000
DOI: 10.1039/C8SC04228D
CC(C)c1ccc(N(Cc2cnn(CCN3CCCCC3)c2)C(=O)C2CCCc3c(OCc4ccccc4)cccc32)cn1
Reaction #305951
5-benzyloxy-N-(6-isopropylpyridin-3-yl)-N-{[1-(2-piperidinoethyl)pyrazol-4-yl]methyl}-1,2,3,4-tetrahydronaphthalene-1-carboxamide
Yield 86.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C(CCl)N1CCC(n2cc3c(n2)CCc2c-3sc3ncnc(Nc4ccc(OCc5cccc(F)c5)c(Cl)c4)c23)CC1
Reaction #309231
desired product
Yield 70.5%DOI: 10.6084/m9.figshare.5104873.v1
Nc1nccn1CCN1CCCCC1
Reaction #309815
oil
Yield 22.6%DOI: 10.6084/m9.figshare.5104873.v1
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