HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 397004Generated: October 29, 2026
2,4,6-Trimethylpyridine → HCID 22943405, compound
https://huagongshe.com/reaction/397004
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,4,6-Trimethylpyridine | HCID 7953 | — |
| Reactant | Phenylmethanesulfonyl chloride | HCID 74740 | — |
| Reactant | HCID 57194514 | HCID 57194514 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 22943405 | HCID 22943405 | — |
Reaction Steps
A stirred solution of ethyl (3-amino-6-methyl-2-oxo-1,2-dihydropyridyl)acetate (0.55 g, 2.6 mmole) and 2,4,6-collidine (1.2 mL, 5.2 mmole) in tetrahydrofuran (10 mL) is cooled in an ice bath. A solution of benzylsulfonyl chloride (0.50 g, 2.6 mmole) in tetrahydrofuran (10 mL) is added over a 15 minute period. After addition is complete, the solution is stirred for 30 minutes at 0° C. The reaction mixture is diluted with ethyl acetate (100 mL), washed with 1.0N HCl (until aqueous layer is pH 1), water (10 mL), saturated sodium bicarbonate (10 mL), and brine (2×10 mL). The organic layer is dried over anhydrous magnesium sulfate, and the solvent is removed. The residue is chromatographed through silica gel using 0:100-20:80 ethyl acetate:dichloromethane as eluent to afford the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06608204B1 |
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| Source dataset | uspto-grants-2003_08 |
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| ORD ID | ord-397ec5d2290642b89a2809a78a9cf2c8 |
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| Source note | uspto-grants-2003_08 |
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