HuagongsheHuagongshe Chemistry Print Report · For research reference only
(6-Bromo-4-chloroquinolin-3-yl)(cyclopropyl)methanone → HCID 66716044, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (6-Bromo-4-chloroquinolin-3-yl)(cyclopropyl)methanone | HCID 66715111 | — |
| Reactant | HCID 66715567 | HCID 66715567 | — |
| Product | HCID 66716044 | HCID 66716044 | 98% |
Reaction Steps
Following General procedure C, (6-bromo-4-chloroquinolin-3-yl)(cyclopropyl)methanone (311 mg, 1 mmol) was reacted with tert-butyl 3-(5-aminopyridin-2-ylamino)pyrrolidine-1-carboxylate (417 mg, 1.5 mmol) to afford the desired product (450 mg, 98%) as a yellow solid: ESI MS m/z 552 [C27H30BrN5O3+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09120749B2 |
| Source dataset | uspto-grants-2015_09 |
| ORD ID | ord-0f4c1d7297ee46a881373b61320d86b4 |
| Source note | uspto-grants-2015_09 |