HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 470392Generated: October 25, 2026
Sodium Carbonate → HCID 67997358, compound
https://huagongshe.com/reaction/470392
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Methyl 2-[(5-bromopyrimidin-4-yl)sulfanyl]acetate | HCID 66318500 | — |
| Reactant | 4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1-naphthonitrile | HCID 67997556 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 67997358 | HCID 67997358 | 53% |
Reaction Steps
A mixture of methyl 2-(5-bromopyrimidin-4-ylthio)acetate (220 mg, 0.84 mmol), 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1-naphthonitrile (237 mg, 0.85 mmol) palladium tetrakis triphenylphoshine (46 mg, 0.04 mmol) and aqueous sodium carbonate solution (2M, 1.5 mL, 3 mmol) in dioxane (3 mL) was heated to 100° C. for 5 hours. The reaction mixture was allowed to cool to room temperature and aqueous sodium hydroxide solution added (1M, 30 mL). The mixture was washed with ethyl acetate (2×20 mL), and the aqueous layer acidified to pH 4 resulting in formation of a precipitate which was isolated by filtration and dried under vacuum to yield 2-(5-(4-cyanonaphthalen-1-yl)pyrimidin-4-ylthio)acetic acid (143 mg, 53%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08629278B2 |
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| Source dataset | uspto-grants-2014_01 |
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| ORD ID | ord-d60a26cff6d84c62ae64d0427a7577b2 |
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| Source note | uspto-grants-2014_01 |
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