HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 28378Generated: October 29, 2026
Triethylamine → HCID 58641490, compound
https://huagongshe.com/reaction/28378
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | HCID 136013282 | HCID 136013282 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 58641490 | HCID 58641490 | — |
Reaction Steps
A solution of ethyl 2-(3-acetoxy-1-chloro-2-(2-hydroxyethoxy)propan-2-yl)-5-hydroxy-6-oxo-1,6-dihydropyrimidine-4-carboxylate (2.322 g, 6.13 mmol) in tetrahydrofuran (100 mL) was treated with methane sulfonylchloride (2.11 g, 18.4 mmol) and Et3N (2.25 g, 22 mmol) and then heated (60° C., oil bath) for 3 hrs. Solvent was removed in-vacuo and the crude product was dissolved in ethyl acetate (100 mL), then washed with water (2×50 mL). The organic solution was dried (Na2SO4), filtered and concentrated in-vacuo to give the title compound as a viscous amber oil which was used immediately in the following reaction.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07419969B2 |
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| Source dataset | uspto-grants-2008_09 |
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| ORD ID | ord-190fd5002d614639b1aa7fa8ddae6656 |
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| Source note | uspto-grants-2008_09 |
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