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 66715867, 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 66715987 | HCID 66715987 | — |
| Product | HCID 66715867 | HCID 66715867 | 20.3% |
Reaction Steps
Following general procedure D, (6-bromo-4-(6-(2-(dimethylamino)ethoxy)pyridin-3-ylamino)quinolin-3-yl)(cyclopropyl)methanone (100 mg, 0.22 mmol) was reacted with 2,6-dichloro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenol (95 mg, 0.33 mmol) to afford the desired product (24 mg, 20%) as a yellow solid: 1H NMR (500 MHz, CD3OD+TFA-d) δ 9.25 (s, 1H), 8.07 (d, J=2.8 Hz, 1H), 7.94 (s, 2H), 7.80 (s, 1H), 7.56 (dd, J=8.5, 2.8 Hz, 1H), 7.18 (s, 2H), 6.93 (d, J=8.5 Hz, 1H), 4.54 (t, J=5.5 Hz, 2H), 3.04 (t, J=5.5 Hz, 2H), 2.95-2.86 (m, 1H), 2.54 (s, 6H), 1.23-1.14 (m, 2H), 1.17-1.08 (m, 2H); ESI MS m/z 537 [C28H26Cl2N4O3+H]+; HPLC>99% (AUC), tR=11.42 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09120749B2 |
| Source dataset | uspto-grants-2015_09 |
| ORD ID | ord-220f9959172a4a80a4af2f88509a38f5 |
| Source note | uspto-grants-2015_09 |