HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl mercaptan → 4-Benzylthio-5-carboxy-2,6-dichloropyrimidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl mercaptan | HCID 7509 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2,4,6-Trichloropyrimidine-5-carboxylic acid | HCID 20083957 | — |
| Solvent | Citric Acid | HCID 311 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-Benzylthio-5-carboxy-2,6-dichloropyrimidine | HCID 17848292 | — |
Reaction Steps
To a mixture of 5-carboxy-2,4,6-trichloropyrimidine (prepared in the above (1)) 100 mg, triethylamine 89 mg in dimethylformamide 3 ml is added at room temperature a 1.0M solution of benzylthiol in tetrahydrofuran 0.44 ml, and the mixture is stirred for 1 hour. The reaction mixture is diluted with a 10% aqueous citric acid solution and extracted with ethyl acetate. The organic layer is washed, dried and concentrated in vacuo to give 4-benzylthio-5-carboxy-2,6-dichloropyrimidine as a pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07273868B2 |
| Source dataset | uspto-grants-2007_09 |
| ORD ID | ord-baa2ccf6fe0d49c3b3cdddb4d97a5c61 |
| Source note | uspto-grants-2007_09 |