HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Cyanophenylboronic acid → (rac)-N-(4-(4-Cyanophenyl)-6,7-dihydro-5H-cyclopenta[c]pyridin-7-yl)propionamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Cyanophenylboronic acid | HCID 2734326 | — |
| Reactant | N-(4-Bromo-6,7-dihydro-5H-cyclopenta[c]pyridin-7-yl)propionamide | HCID 86685956 | — |
| Product | (rac)-N-(4-(4-Cyanophenyl)-6,7-dihydro-5H-cyclopenta[c]pyridin-7-yl)propionamide | HCID 71811408 | 79% |
Reaction Steps
In analogy to the procedure described for the preparation of example 1, (rac)-N-(4-bromo-6,7-dihydro-5H-cyclopenta[c]pyridin-7-yl)propionamide (intermediate A-4) was reacted with 4-cyanophenylboronic acid to give the title compound as light green powder in 79% yield. MS: 292.1 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09187429B2 |
| Source dataset | uspto-grants-2015_11 |
| ORD ID | ord-db47630ecd9540de822e92238ba9b3e5 |
| Source note | uspto-grants-2015_11 |