HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1780296Generated: October 29, 2026
Sodium Carbonate → 3-((S)-1-Methyl-pyrrolidin-2-ylmethoxy)-5-naphthalen-1-yl-pyridine
https://huagongshe.com/reaction/1780296
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 1-Naphthaleneboronic acid | HCID 254532 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 3-Bromo-5-((S)-1-methyl-pyrrolidin-2-ylmethoxy)-pyridine | HCID 11288721 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-((S)-1-Methyl-pyrrolidin-2-ylmethoxy)-5-naphthalen-1-yl-pyridine | HCID 10426041 | 62% |
Reaction Steps
To a solution of 5-bromo-3-(1-methyl-2-(S)-pyrrolidinylmethoxy)-pyridine (272 mg, 1.00 mmol) in benzene (2.0 mL) were added aqueous sodium carbonate (2.0M, 1.0 mL), tetrakis(triphenylphosphine)palladium(0) (35 mg, 0.03 mmol) and 1-naphthaleneboronic acid (189 mg, 1.10 mmol). The reaction mixture was refluxed overnight, then cooled to room temperature. Water (2 mL) was added, and solid sodium bicarbonate was added until the aqueous layer was saturated. The mixture was extracted with EtOAc, which was dried over MgSO4, filtered and concentrated. The residue was chromatographed on a silica gel column, eluting with NH4OH/MeOH/EtOAc 0:1:9 and 1:10:90 to afford a light yellowish oil (196 mg, 62%). MS (CI/NH3) m/z 319 (M+H)+. 1H NMR (CDCl3, 300 MHz) δ1.71-1.92 (m, 3H), 2.00-2.10 (m, 1H), 2.27-2.38 (m, 1H), 2.51 (s, 3H), 2.66-2.75 (m, 1H), 3.09-3.17 (m, 1H), 3.98-4.14 (m, 2H), 7.34-7.57 (m, 5H), 7.72-7.96 (m, 3H), 8.36-8.43 (m, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05629325 |
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| Source dataset | uspto-grants-1997_05 |
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| ORD ID | ord-7d1354cd2d6d4a94be5fb82b4a87b3de |
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| Source note | uspto-grants-1997_05 |
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