HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1519345Generated: November 4, 2026
2-Methoxyphenylboronic acid → HCID 71535532, compound
https://huagongshe.com/reaction/1519345
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Methoxyphenylboronic acid | HCID 2733958 | — |
| Reactant | Methyl 2-bromo-5-(4-(3,4-dichlorophenyl)thiazol-2-yl)benzoate | HCID 86679833 | — |
| Product | HCID 71535532 | HCID 71535532 | 39.4% |
Reaction Steps
Using the conditions of General Procedure B for Suzuki Coupling and Hydrolysis in Parallel Mode, 2-bromo-5-[4-(3,4-dichloro-phenyl)-thiazol-2-yl]-benzoic acid methyl ester (which may be prepared as described for Intermediate 6; 89 mg, 0.2 mmol) was reacted with 2-methoxyphenylboronic acid (available from Frontier Scientific, Inc.; 61 mg, 0.4 mmol). The resulting ester was hydrolyzed and the acid was purified to give 4-[4-(3,4-dichloro-phenyl)-thiazol-2-yl]-2′-methoxy-biphenyl-2-carboxylic acid (36 mg, 39%). 1H NMR (400 MHz, DMSO-d6) δ 12.75 (br s, 1H), 8.45 (s, 1H), 8.31-8.37 (m, 2H), 8.21 (d, J=8.0 Hz, 1H), 8.09 (d, J=8.3 Hz, 1H), 7.77 (d, J=8.5 Hz, 1H), 7.46 (d, J=8.0 Hz, 1H), 7.36 (t, J=7.8 Hz, 1H), 7.27 (d, J=7.5 Hz, 1H), 7.04 (d, J=7.3 Hz, 2H), 3.69 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09073881B2 |
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| Source dataset | uspto-grants-2015_07 |
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| ORD ID | ord-9e878f7d900646ec8db672c5a72454ad |
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| Source note | uspto-grants-2015_07 |
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