HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 66715437, compound → HCID 66715790, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 66715437 | HCID 66715437 | — |
| Reactant | 2-Chloro-6-fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenol | HCID 66716079 | — |
| Product | HCID 66715790 | HCID 66715790 | 24.1% |
Reaction Steps
Following general procedure D, ((6-bromo-4-(4-((dimethylamino)methyl)phenylamino)-7-fluoroquinolin-3-yl)(cyclopropyl)methanone (40 mg, 0.090 mmol) was reacted with 2-chloro-6-fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenol (31 mg, 0.113 mmol) to afford the desired product (11 mg, 24%) as a yellow solid: 1H NMR (500 MHz, DMSO-d6) δ 10.70 (s, 1H), 9.06 (s, 1H), 8.09 (d, J=8.5 Hz, 1H), 7.75 (d, J=12 Hz, 1H), 7.26 (d, J=8.5 Hz, 2H), 7.21 (d, J=6.5 Hz, 2H), 7.09 (d, J=8.5, 2H), 3.40 (s, 2H), 2.77 (quint, J=15 Hz, 1H), 2.13 (s, 6H), 0.86 (m, 4H); ESI MS m/z 508, [C28H24ClF2N3O2+H]+; HPLC 98.7% (AUC), tR=10.83 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09120749B2 |
| Source dataset | uspto-grants-2015_09 |
| ORD ID | ord-cd1b77f2cae94796b51ce4bb8db09432 |
| Source note | uspto-grants-2015_09 |