HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1032216Generated: October 30, 2026
N,N-Dimethylaniline → 5-Acetoxymethyl7-chloro-2-methyl-s-triazolo[1,5-a]pyrimidine
https://huagongshe.com/reaction/1032216
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N,N-Dimethylaniline | HCID 949 | — |
| Reactant | Chloroform | HCID 6212 | — |
| Reactant | HCID 178475878 | HCID 178475878 | — |
| Solvent | Phosphorus oxychloride | HCID 24813 | — |
| Product | 5-Acetoxymethyl7-chloro-2-methyl-s-triazolo[1,5-a]pyrimidine | HCID 15672776 | — |
Reaction Steps
In 300 ml of phosphorus oxychloride was added dropwise 40 ml of N,N-dimethylaniline, and 35 g of 5-acetoxymethyl-7-hydroxy-2-methyl-s-triazolo[1,5-a]pyrimidine was added to the mixture and the mixture was stirred at 50° C. for one hour. An oily residue obtained by removing phosphorus oxychloride was dissolved in 500 ml of chloroform and ice-cooled. After addition of crushed ice and water to the mixture and stirring thereof, a chloroform layer was separated, washed with water and dried over anhydrous magnesium sulfate. Then, removing a solvent, an oily product was obtained. This was applied to a silica gel column chromatography (eluent: chloroform) and fractions containing the title compound were condensed to obtain an oily product. This was allowed to stand to cool and crystallized to obtain 31 g of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04956462 |
|---|
| Source dataset | uspto-grants-1990_09 |
|---|
| ORD ID | ord-08bd3a79e2874e47bbe67b381fdd5f03 |
|---|
| Source note | uspto-grants-1990_09 |
|---|