HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 356867Generated: October 30, 2026
Triethylamine → Methyl 3-benzyloxy-3-phenyl-2-(4,6-dimethoxypyrimidin-2-ylthio)-butyrate
https://huagongshe.com/reaction/356867
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | Methyl 3-benzyloxy-3-phenyl-2-hydroxybutyrate | HCID 15292268 | — |
| Reactant | Sodium dimethylformamide | HCID 86746767 | — |
| Reactant | HCID 178493561 | HCID 178493561 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Methyl 3-benzyloxy-3-phenyl-2-(4,6-dimethoxypyrimidin-2-ylthio)-butyrate | HCID 15292275 | 29% |
Reaction Steps
11 g (25 mmol) of methyl 3-benzyloxy-3-phenyl-2-hydroxybutyrate (comp. 1.1) are dissolved in 50 ml of dichloromethane, 3 g (30 mmol) of triethylamine are added and, while stirring, 3.2 g (28 mmol) of methanesulfonyl chloride are added dropwise. The mixture is stirred at room temperature for 2 hours, washed with water, dried over magnesium sulfate and concentrated under reduced pressure. The residue is taken up in DMF and added dropwise to a suspension of 12.9 g (75 mmol) of 4,6-dimethoxypyrimidine-2-thiol and 8.4 g (100 nmol) of sodium DMF at 0° C. After stirring at room temperature for 2 hours and at 60° C. for a further 2 hours, the mixture is poured into 1 1 of ice-water, and the precipitate is filtered off with suction. Drying results in 3.2 g of a white powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05840722 |
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| Source dataset | uspto-grants-1998_11 |
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| ORD ID | ord-3cfcf8f88c6248a289a5131a0e00c216 |
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| Source note | uspto-grants-1998_11 |
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