HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-Acetyl-2-chlorophenylboronic acid → HCID 86679860, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-Acetyl-2-chlorophenylboronic acid | HCID 2763246 | — |
| Reactant | Methyl 2-bromo-5-(4-(3,4-dichlorophenyl)thiazol-2-yl)benzoate | HCID 86679833 | — |
| Product | HCID 86679860 | HCID 86679860 | 7% |
Reaction Steps
5′-Acetyl-2′-chloro-4-[4-(3,4-dichloro-phenyl)-thiazol-2-yl]-biphenyl-2-carboxylic acid was prepared in 7% yield (for two steps) from 2-bromo-5-[4-(3,4-dichloro-phenyl)-thiazol-2-yl]-benzoic acid methyl ester (which may be prepared as described for Intermediate 6) and 5-acetyl-2-chlorophenylboronic acid (available from Combi-Blocks Inc.) using General Procedure A for Suzuki Coupling and Hydrolysis in Parallel Mode. 1H NMR (300 MHz, DMSO-d6) δ 13.14 (s, 1H), 8.58 (d, J=1.9 Hz, 1H), 8.50 (s, 1H), 8.30-8.38 (m, 2H), 8.10 (dd, J=8.4, 2.0 Hz, 1H), 7.98 (dd, J=8.3, 2.1 Hz, 1H), 7.90 (d, J=2.1 Hz, 1H), 7.78 (d, J=8.5 Hz, 1H), 7.69 (d, J=8.5 Hz, 1H), 7.51 (d, J=8.1 Hz, 1H), 2.62 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09073881B2 |
| Source dataset | uspto-grants-2015_07 |
| ORD ID | ord-b290ae4889d240978420735862ef9968 |
| Source note | uspto-grants-2015_07 |