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 178450276, 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 178450269 | HCID 178450269 | — |
| Product | HCID 178450276 | HCID 178450276 | 35.3% |
Reaction Steps
Following general procedure A-1, 1-{6-bromo-4-[trans-4-((dimethylamino)methyl)cyclohexylamino]quinolin-3-yl}butan-1-one (48 mg, 0.110 mmol) was reacted with 2,6-dichloro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenol (47 mg, 0.165 mmol) to afford the desired product (20 mg, 35%) as a yellow solid: 1H NMR (500 MHz, CD3OD+TFA-d) δ 9.14 (s, 1H), 8.47 (s, 1H), 8.27 (dd, J=8.7, 1.8 Hz, 1H), 8.98 (d, J=8.7 Hz, 1H), 7.72 (s, 2H), 4.53 (s, 1H), 3.16-3.06 (m, 4H), 2.94 (s, 6H), 2.50-2.43 (m, 2H), 2.08-2.02 (m, 3H), 1.88-1.74 (m, 4H), 1.39-1.32 (m, 1H), 1.06 (t, J=7.4 Hz, 3H); ESI MS m/z 514 [C28H33Cl2N3O2+H]+; HPLC 98.7% (AUC), tR=11.27 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09120749B2 |
| Source dataset | uspto-grants-2015_09 |
| ORD ID | ord-727b78564dc44fecbebf7aede1b87d4b |
| Source note | uspto-grants-2015_09 |