HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,6-Dichloro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenol → HCID 66716647, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,6-Dichloro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenol | HCID 66715127 | — |
| Reactant | HCID 68091904 | HCID 68091904 | — |
| Product | HCID 66716647 | HCID 66716647 | 83% |
Reaction Steps
Following general procedure D, {6-bromo-4-[4-((4-methylpiperazin-1-yl)methyl)phenylamino]quinolin-3-yl}(cyclopropyl)methanone (42 mg, 0.088 mmol) was reacted with 2,6-dichloro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenol (38 mg, 0.132 mmol) to afford the desired product (41 mg, 83%) as a yellow solid: 1H NMR (300 MHz, CD3OD) δ 9.27 (s, 1H), 7.93-7.85 (m, 2H), 7.74 (s, 1H), 7.37 (d, J=8.1 Hz, 2H), 7.19-7.10 (m, 4H), 3.61 (s, 2H), 2.95-2.88 (m, 1H), 2.74-2.68 (m, 4H), 2.57-2.46 (m, 7H), 1.23-1.10 (m, 4H); ESI MS m/z 561 [C31H30Cl2N4O2+H]+; HPLC 94.4% (AUC), tR=8.57 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09120749B2 |
| Source dataset | uspto-grants-2015_09 |
| ORD ID | ord-cbb27805a9964c548e703065ae3a2eb0 |
| Source note | uspto-grants-2015_09 |