HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 378365Generated: October 29, 2026
Triethylamine → Methyl 3-phenoxy-3-phenyl-2-[(4,6-dimethoxy-2-pyrimidinyl)thio]butyrate
https://huagongshe.com/reaction/378365
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Methyl 3-benzyloxy-3-phenyl-2-hydroxybutyrate | HCID 15292268 | — |
| Reactant | HCID 178493561 | HCID 178493561 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Methyl 3-phenoxy-3-phenyl-2-[(4,6-dimethoxy-2-pyrimidinyl)thio]butyrate | HCID 15292300 | 38.1% |
Reaction Steps
7.2 g (25 mmol) of methyl 3-phenoxy-3-phenyl-2-hydroxybutyrate (Compound 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 100 mo of DMF and added dropwise to a suspension 12.9 g (75 mmol) of 4,6-dimethoxypyrimidine-2-thiol and 8.4 g (100 mmol) sodium bicarbonate in 100 ml of DMF at 0° C. After stirring at room temperature for 2 hours and at 60° C. for further 2 hours, the mixture is poured into 1 liter of ice-water, and the precipitate is filtered off with suction. Drying results in 4.2 g of a white powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06030975 |
|---|
| Source dataset | uspto-grants-2000_02 |
|---|
| ORD ID | ord-51f43ff620c64095b90bfe1cffaab82a |
|---|
| Source note | uspto-grants-2000_02 |
|---|