HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 601783Generated: October 29, 2026
2,6-Dimethoxypyridine → HCID 57517884, compound
https://huagongshe.com/reaction/601783
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,6-Dimethoxypyridine | HCID 80378 | — |
| Reactant | 5-chloro-1H-indole-2,3-dione | HCID 87203 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 57517884 | HCID 57517884 | 71.1% |
Reaction Steps
To a stirred solution of 2,6-dimethoxypyridine (50 mmol, 6.61 mL) in THF (100 mL) was added slowly a 1.6 M solution of n-butyllithium in hexanes (55 mmol, 34.4 mL) at −78° C. The mixture was allowed to warm slowly to 10° C. and kept at this temperature for 30 min. The reaction mixture was re-cooled to −78° C. and a slurry of 5-chloroisatin (20 mmol, 3.63 g) in THF (150 mL) was added portionwise, keeping the temperature below −60° C. The reaction was allowed to come to room temperature. The mixture was quenched with 10% aqueous ammonium chloride solution and extracted several times with ethyl acetate. The combined organic layers were washed with water, dried over magnesium sulfate and evaporated in vacuo. Recrystallization from ethyl acetate yielded 4.56 g (71%) of the desired intermediate as a white crystalline solid (71%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07902379B2 |
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| Source dataset | uspto-grants-2011_03 |
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| ORD ID | ord-dbfae02b1e8f4b51837c6db20d4e2342 |
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| Source note | uspto-grants-2011_03 |
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