HuagongsheHuagongshe Chemistry Print Report · For research reference only
(6-Bromo-4-chloroquinolin-3-yl)(cyclopropyl)methanone → HCID 66715668, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (6-Bromo-4-chloroquinolin-3-yl)(cyclopropyl)methanone | HCID 66715111 | — |
| Reactant | HCID 66715324 | HCID 66715324 | — |
| Product | HCID 66715668 | HCID 66715668 | 63% |
Reaction Steps
Following General procedure C, (6-bromo-4-chloroquinolin-3-yl)(cyclopropyl)methanone (311 mg, 1 mmol) was reacted with tert-butyl 2-(5-aminopyridin-2-yloxy)ethylcarbamate (380 mg, 1.5 mmol) to afford the desired product (332 mg, 63%) as a yellow solid: ESI MS m/z 527 [C25H27BrN4O4+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09120749B2 |
| Source dataset | uspto-grants-2015_09 |
| ORD ID | ord-1fa7b2698a34420798086aee165d9f9a |
| Source note | uspto-grants-2015_09 |