Teilstruktursuche

792348

CN1CCC(C23OC(O)(Cc4cc(Cl)ccc42)c2cccnc23)CC1

Reaction #49691

8-Chloro-6,11-dihydro-11-(1-methyl-4-piperidinyl)-5,11-epoxy-5H-benzo[5,6]-cyclohepta[1,2-b]pyridin-5-ol

DOI: 10.6084/m9.figshare.5104873.v1

CCn1ncc2c(Cl)c3c(nc21)C(O)(C1CCN(C)CC1)c1ccccc1CC3

Reaction #391920

DOI: 10.1039/C8SC04228D

CN1CCC(C2(O)c3ccc(C#N)cc3CCc3cccnc32)CC1

Reaction #571489

8-cyano-6,11-dihydro-11-(1-methyl-4-piperidyl)-5H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ol

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

CSc1ccc2c(c1)CCc1cccnc1C2=C1CCN(C)CC1

Reaction #571491

8-methylthio-11-(1-methyl-4-piperidylidene)-6,11-dihydro-5H-benzo[5,6]cyclohepta[1,2-b]pyridine

Ausbeute 61.4%DOI: 10.6084/m9.figshare.5104873.v1

CN1CCC(C2(O)c3ccc(S(C)(=O)=O)cc3CCc3cccnc32)CC1

Reaction #571492

8-methylsulfonyl-6,11-dihydro-11-(1-methyl-4-piperidyl)-5H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ol

Ausbeute 61.0%DOI: 10.6084/m9.figshare.5104873.v1

CN1CCC(=C2c3ccc(C#N)cc3CCc3cccnc32)CC1

Reaction #571493

8-cyano-11-(1-methyl-4-piperidylidene)-6,11-dihydro-5H-benzo[5,6]cyclohepta[1,2-b]pyridine

Ausbeute 63.0%DOI: 10.6084/m9.figshare.5104873.v1

CN1CCC(=C2c3ccc(S(C)(=O)=O)cc3CCc3cccnc32)CC1

Reaction #571495

8-Methylsulfonyl-11-(1-methyl-4-piperidylidene)-6,11-dihydro-5H-benzo[5,6]cyclohepta[1,2-b]pyridine

Ausbeute 74.0%DOI: 10.6084/m9.figshare.5104873.v1

CSc1ccc2c(c1)CCc1cccnc1C2=C1CCN(C)CC1

Reaction #770604

DOI: 10.1039/C8SC04228D

Reaction #1464752

DOI: 10.6084/m9.figshare.5104873.v1

$CC1C/C(=C2\c3ccc(Cl)cc3CCc3cccnc32)C(C)CN1$

Reaction #1464754

Ausbeute 6.3%DOI: 10.6084/m9.figshare.5104873.v1

CCn1ncc2c(Cl)c3c(nc21)C(O)(C1CCN(C)CC1)c1ccccc1CC3

Reaction #1535334

4-chloro-1-ethyl-1,5,6,11-tetrahydro-11-(1-methyl-4-piperidinyl)benzo[5,6]cyclohepta[1,2-b]pyrazolo[4,3-e]pyridin-11-ol

DOI: 10.6084/m9.figshare.5104873.v1

CN1CCC(C2(O)c3ccc(Cl)cc3CC(=O)c3cccnc32)CC1

Reaction #1621767

8-chloro-11-hydroxy-11-(1-methyl-4-piperidinyl)-6,11-dihydro-5H-benzo[5,6]cyclohepta[1,2-b]pyridin-5-one

DOI: 10.6084/m9.figshare.5104873.v1

CN1CCC(C(O)c2ncccc2CCc2ccccc2)CC1

Reaction #1621772

Ausbeute 87.5%DOI: 10.6084/m9.figshare.5104873.v1

CN1CCC(=C2c3ccc(C#N)cc3CCc3cccnc32)CC1

Reaction #1646459

DOI: 10.1039/C8SC04228D

Reaction #1842865

DOI: 10.6084/m9.figshare.5104873.v1

Reaction #1850441

Grignard reagent

DOI: 10.6084/m9.figshare.5104873.v1

CN1CCC(C23OC(O)(Cc4cc(Cl)ccc42)c2cccnc23)CC1

Reaction #1973610

8-Chloro-6,11-dihydro-11-(1-methyl-4-piperidinyl)-5,11-epoxy-5H-benzo[5,6]-cyclohepta[1,2-b]pyridin-5-ol

DOI: 10.6084/m9.figshare.5104873.v1