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 178484100, 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 178484099 | HCID 178484099 | — |
| Product | HCID 178484100 | HCID 178484100 | 90% |
Reaction Steps
Following general procedure F, {6-bromo-4-[trans-4-(dimethylamino)cyclohexylamino]-7-fluoroquinolin-3-yl}(cyclopropyl)methanone (38 mg, 0.087 mmol) was reacted with 2-chloro-6-fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenol (35 mg, 0.131 mmol) to afford the desired product (39 mg, 90%) as a green solid: 1H NMR (300 MHz, CD3OD) δ 9.19 (s, 1H), 8.29 (d, J=8.1 Hz, 1H), 7.60 (d, J=11.8 Hz, 1H), 7.49 (s, 1H), 7.42 (dt, J=11.6, 2.0 Hz, 1H), 4.18 (s, 1H), 2.86 (s, 6H), 2.85-2.78 (m, 1H), 2.42 (s, 2H), 2.19 (s, 2H), 1.76-1.62 (m, 4H), 1.22-1.07 (m, 5H); ESI MS m/z 500 [C27H28ClF2N3O2+H]+; HPLC 97.4% (AUC), tR=9.21 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09120749B2 |
| Source dataset | uspto-grants-2015_09 |
| ORD ID | ord-8a3e074802d941b2a7cdf1fbb158c709 |
| Source note | uspto-grants-2015_09 |