HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Chloro-6-fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenol → HCID 68298741, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Chloro-6-fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenol | HCID 66716079 | — |
| Reactant | HCID 68092005 | HCID 68092005 | — |
| Product | HCID 68298741 | HCID 68298741 | 74% |
Reaction Steps
Following general procedure F, {6-Bromo-4-[1-(1-methylpiperidin-3-yl)-1H-pyrazol-4-ylamino]quinolin-3-yl}(cyclopropyl)methanone (58 mg, 0.120 mmol) was reacted with 2-chloro-6-fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenol (49 mg, 0.180 mmol) to afford the desired product (46 mg, 74%) as a yellow-green solid: 1H NMR (500 MHz, DMSO-d6) δ 10.86 (s, 1H), 9.08 (s, 1H), 8.24 (d, J=2.1 Hz, 1H), 8.04 (dd, J=8.8, 2.1 Hz, 1H), 7.93-7.83 (m, 2H), 7.43 (s, 1H), 7.39-7.30 (m, 2H), 4.19-4.12 (m, 1H), 2.95-2.81 (m, 3H), 2.29-2.15 (s, 5H), 2.01-1.89 (m, 4H), 1.02-0.92 (m, 4H).; ESI MS m/z 520 [C28H27ClFN5O2+H]+; HPLC 98.6% (AUC), tR=10.16 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09120749B2 |
| Source dataset | uspto-grants-2015_09 |
| ORD ID | ord-be020e0cd1f44b4daa788eb8b04672a1 |
| Source note | uspto-grants-2015_09 |