Submission Details

Molecule(s):
O=C(CCl)N1CCN(S(=O)(=O)c2ccc(F)cc2)CC1

DRR-IMP-dff87f5e-1
Duplicate of:
KAY-MCD-d0fe5261-1

O=C(CCl)N1CCN(S(=O)(=O)c2ccc(F)cc2)CC1

Duplicate piperazine-chloroacetamide Check Availability on Manifold View
O=C(CCl)N1CCN(S(=O)(=O)c2ccc3ccccc3c2)CC1

DRR-IMP-dff87f5e-2
Duplicate of:
MAK-UNK-7c9d1431-3

O=C(CCl)N1CCN(S(=O)(=O)c2ccc3ccccc3c2)CC1

Duplicate piperazine-chloroacetamide Check Availability on Manifold View
O=C(CCl)N1CCN(S(=O)(=O)c2ccc(Cl)cc2)CC1

DRR-IMP-dff87f5e-3
Duplicate of:
AAR-POS-d2a4d1df-44

O=C(CCl)N1CCN(S(=O)(=O)c2ccc(Cl)cc2)CC1

Duplicate piperazine-chloroacetamide Made Check Availability on Manifold View
O=C(CCl)N1CCN(S(=O)(=O)c2c(Cl)cccc2Cl)CC1

DRR-IMP-dff87f5e-4

O=C(CCl)N1CCN(S(=O)(=O)c2c(Cl)cccc2Cl)CC1

O=C(CCl)N1CCN(S(=O)(=O)c2ccccc2F)CC1

DRR-IMP-dff87f5e-5
Duplicate of:
AAR-POS-d2a4d1df-34

O=C(CCl)N1CCN(S(=O)(=O)c2ccccc2F)CC1

Duplicate piperazine-chloroacetamide Made Check Availability on Manifold View
O=C(CCl)N1CCN(S(=O)(=O)c2ccc(C(F)(F)F)cc2)CC1

DRR-IMP-dff87f5e-6

O=C(CCl)N1CCN(S(=O)(=O)c2ccc(C(F)(F)F)cc2)CC1

O=C(CCl)N1CCN(S(=O)(=O)c2ccc(Br)cc2)CC1

DRR-IMP-dff87f5e-7

O=C(CCl)N1CCN(S(=O)(=O)c2ccc(Br)cc2)CC1

O=C(CCl)N1CCN(S(=O)(=O)c2cccc(Cl)c2)CC1

DRR-IMP-dff87f5e-8

O=C(CCl)N1CCN(S(=O)(=O)c2cccc(Cl)c2)CC1

N#Cc1ccc(S(=O)(=O)N2CCN(C(=O)CCl)CC2)cc1

DRR-IMP-dff87f5e-9

N#Cc1ccc(S(=O)(=O)N2CCN(C(=O)CCl)CC2)cc1


Design Rationale:

We have studied, in collaboration with Ben Perry at the DNDi, the SAR available on the piperazine-chloroacetamide series. My current Masters student has synthesized these 9 molecules.

Other Notes:

Previous Masters student also worked on this series. Synthesis is very straightforward and reliable.

Inspired By:
Discussion: