HuagongsheHuagongshe Chemistry Print Report · For research reference only
(6-Bromo-4-chloroquinolin-3-yl)(cyclopropyl)methanone → HCID 66715852, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (6-Bromo-4-chloroquinolin-3-yl)(cyclopropyl)methanone | HCID 66715111 | — |
| Reactant | HCID 66715594 | HCID 66715594 | — |
| Product | HCID 66715852 | HCID 66715852 | 69% |
Reaction Steps
Following General procedure C, (6-bromo-4-chloroquinolin-3-yl)(cyclopropyl)methanone (239 mg, 0.8 mmol) was reacted with tert-butyl 3-(5-aminopyridin-2-ylamino)piperidine-1-carboxylate (337 mg, 1.1 mmol) to afford the desired product (300 mg, 69%) as a yellow solid: ESI MS m/z 566 [C28H32BrN5O3+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09120749B2 |
| Source dataset | uspto-grants-2015_09 |
| ORD ID | ord-6df8b6eb2b28464695cd605479708703 |
| Source note | uspto-grants-2015_09 |