HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 397010Generated: October 28, 2026
2,4,6-Trimethylpyridine → Ethyl 5-benzylsulfonylamino-1-methoxymethyl-3-uracilylacetate
https://huagongshe.com/reaction/397010
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2,4,6-Trimethylpyridine | HCID 7953 | — |
| Reactant | Phenylmethanesulfonyl chloride | HCID 74740 | — |
| Reactant | Ethyl 5-amino-1-methoxymethyluracilylacetate | HCID 54496358 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Ethyl 5-benzylsulfonylamino-1-methoxymethyl-3-uracilylacetate | HCID 22943410 | — |
Reaction Steps
A stirred solution of ethyl 5-amino-1-methoxymethyl-uracilylacetate (8.0 g, 31 mmole) and 2,4,6-collidine (13.7 mL, 62 mmole) in tetrahydrofuran (50 mL) is cooled in an ice bath. A solution of benzylsulfonyl chloride (5.93 g, 31 mmole) in tetrahydrofuran (50 mL) is added over a 30-minute period. After addition is complete, the solution is stirred for 1 hour at 0° C., then 3 hours at room temperature. The reaction mixture is diluted with ethyl acetate, washed with 1.0N HCl (until aqueous layer is pH 1), water, saturated sodium bicarbonate, and brine. The organic layer is dried over anhydrous magnesium sulfate, and the solvent is removed. The title compound is isolated.
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-83c86f7ff8e04d0fa620a4b2ef1ac2b7 |
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| Source note | uspto-grants-2003_08 |
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