子结构搜索

3082

Cc1c(N2CCN(c3ccccn3)CC2)c(F)cn2c(=O)c(C(=O)O)cc(C3CC3)c12

DOI: 10.6084/m9.figshare.5104873.v1

COc1cc(C(=O)CN2CCN(c3ccncc3)CC2)ccc1OCC(=O)O

收率 47.0%DOI: 10.6084/m9.figshare.5104873.v1

COC(=O)Cc1ccc(C(=O)CN2CCN(c3ccncc3)CC2)cc1

DOI: 10.6084/m9.figshare.5104873.v1

CC(C)OC(=O)COc1ccc(C(=O)CN2CCN(c3ccncc3)CC2)cc1

DOI: 10.6084/m9.figshare.5104873.v1

COC(=O)COc1ccc(C(=O)C(C)CN2CCN(c3ccncc3)CC2)cc1

DOI: 10.6084/m9.figshare.5104873.v1

NC(CC(=O)c1ccc(N2CCN(c3ccncc3)CC2)cc1)C(=O)O

DOI: 10.6084/m9.figshare.5104873.v1

Cl.O=C(O)CCCOc1ccc(N2CCN(c3ccncc3)CC2)cc1

收率 81.3%DOI: 10.6084/m9.figshare.5104873.v1

Cl.O=C(O)COc1ccc(C(=O)CN2CCN(c3ccncc3)CC2=O)cc1

收率 40.7%DOI: 10.6084/m9.figshare.5104873.v1

C=CC(COc1ccc(N2CCN(c3ccncc3)CC2)cc1)CC(=O)OC

methyl 4-[4-[4-(4-pyridyl)piperazin-1-yl]-phenoxy]-3-vinylbutyrate

收率 19.6%DOI: 10.6084/m9.figshare.5104873.v1

COC(=O)C(N)CCOc1ccc(N2CCN(c3ccncc3)CC2)cc1

收率 74.1%DOI: 10.6084/m9.figshare.5104873.v1

CCOC(=O)COc1ccc(C(=O)CN2CCN(c3ccncc3)CC2=O)cc1

DOI: 10.6084/m9.figshare.5104873.v1

Reaction #77537

收率 73.0%DOI: 10.6084/m9.figshare.5104873.v1

Reaction #77548

收率 37.0%DOI: 10.6084/m9.figshare.5104873.v1

Reaction #77550

收率 45.0%DOI: 10.6084/m9.figshare.5104873.v1

Cc1cc(N2CCCC2)c2ccc(OCc3ccc(C#N)cc3)cc2n1

Reaction #178113

DOI: 10.1039/C8SC04228D

CC(=O)c1ccc(N2CCN(c3ccncc3)CC2)cc1

Reaction #190853

DOI: 10.1039/C8SC04228D

Cc1cc(N2CCC(NN3C(=O)CN(S(=O)(=O)c4ccc5cc(Cl)ccc5c4)CC3CC(N)=O)CC2)ccn1

Reaction #197464

DOI: 10.1039/C8SC04228D

N=C(Nc1ccc(F)cc1)N1CCN(c2ccnc3cc(Cl)ccc23)CC1

Reaction #202010

DOI: 10.1039/C8SC04228D

Cn1c(=O)c(C#N)c(N2CCN(C(=O)c3ccco3)CC2)c2cc(Cl)ccc21

Reaction #205640

DOI: 10.1039/C8SC04228D

COC1CCCCC(NC(=O)N2CCN(c3ccnc4cc(Cl)ccc34)CC2)C1

Reaction #209116

DOI: 10.1039/C8SC04228D

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