HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 1-(4-Methylthiazol-2-ylsulfonyloxy)-1,2,3-benzotriazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | 4-methyl-1,3-thiazole-2-sulfonyl Chloride | HCID 11680007 | — |
| Solvent | tert-Butyl methyl ether | HCID 15413 | — |
| Product | 1-(4-Methylthiazol-2-ylsulfonyloxy)-1,2,3-benzotriazole | HCID 17864614 | — |
Reaction Steps
Under atmosphere of argon, to a solution of 4-methylthiazol-2-sulfonyl chloride in methyl t-butyl ether (0.20 M, 20 ml), 1-hydroxybenzotriazole (549 mg) and triethylamine (0.57 ml) were added under stirring with cooled on ice bath, and the mixture was stirred for 1 hour at room temperature. To the reaction mixture, ethyl acetate was added. The organic layer was washed with water three times, with a saturated aqueous solution of sodium chloride once successively, dried over an anhydrous magnesium sulfate and concentrated to give the compound of the present invention (1.1 g) having the following physical data.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08088802B2 |
| Source dataset | uspto-grants-2012_01 |
| ORD ID | ord-b417ef1ede6a42f4ba942132ac7d4b64 |
| Source note | uspto-grants-2012_01 |