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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1519367Generated: November 1, 2026

5-Acetyl-2-chlorophenylboronic acid → HCID 86679860, compound

https://huagongshe.com/reaction/1519367

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Acetyl-2-chlorophenylboronic acidHCID 2763246—
ReactantMethyl 2-bromo-5-(4-(3,4-dichlorophenyl)thiazol-2-yl)benzoateHCID 86679833—
ProductHCID 86679860HCID 866798607%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09073881B2
Source datasetuspto-grants-2015_07
ORD IDord-b290ae4889d240978420735862ef9968
Source noteuspto-grants-2015_07