HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → HCID 20275273, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | HCID 20275265 | HCID 20275265 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 20275273 | HCID 20275273 | — |
Reaction Steps
A mixture of 1.2 g (5 mmole) of 7-chloro-2-hydroxy-5-methylthiotriazolo[1,5-c]pyrimidine (from Example 7), 2 g (14 mmole) of methyl iodide, 1.2 g (5 mmole) of sodium methoxide (as a 25% methanolic solution), and 50 ml of methanol was heated at its reflux temperature for two hours and then cooled. The solid was collected by filtration and recrystallized from a 50:50 mixture of glyme and hexane to provide yellow crystals of 7-chloro-2-methoxy-5-methylthiotriazolo[1,5-c]pyrimidine, m.p. 243°-244° C. Analysis: Calculated for C7H7ClN4OS: %C, 36.4; %H, 3.1; %N, 24.3; Found: %C, 36.3; %H, 2.9; %N, 24.2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04528288 |
| Source dataset | uspto-grants-1985_07 |
| ORD ID | ord-5c3c9cff0cd0481c99954e0cc2f9cd48 |
| Source note | uspto-grants-1985_07 |