HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 643001Generated: November 1, 2026
(2-Methoxypyridin-3-yl)boronic acid → HCID 86614001, compound
https://huagongshe.com/reaction/643001
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | (2-Methoxypyridin-3-yl)boronic acid | HCID 2762709 | — |
| Reactant | HCID 86614002 | HCID 86614002 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 86614001 | HCID 86614001 | — |
Reaction Steps
A mixture of 5-chloro-N-((1-(4-iodophenyl-1H-imidazol-4-yl)methyl)thiophene-2-carboxamide (0.044 g, 0.1 mmol), 2-methoxypyridine-3-ylboronic acid (0.016 g, 0.11 mmol) and Pd(PPh3)2Cl2 (0.007 g, 0.01 mmol) in p-dioxane (0.7 mL) was purged with Argon for 5 min. A degassed aqueous solution of Na2CO3 (IM, 0.3 mL) was added. After being heated at 100° C. for 2 h, the mixture was cooled to room temperature, and purified by preparative HPLC to yield 5-chloro-N-((1-(4-(2-methoxypyridin-3-yl)phenyl-1H-imidazol-4-yl)methyl)thiophene-2-carboxamide (MS 425.0, 427.0 (M+H), Cl pattern).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07696352B2 |
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| Source dataset | uspto-grants-2010_04 |
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| ORD ID | ord-26b86d36fc3447ed84e79ec30215abfa |
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| Source note | uspto-grants-2010_04 |
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