HuagongsheHuagongshe Chemistry Print Report · For research reference only
Iodoethane → HCID 21984910, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | HCID 178462984 | HCID 178462984 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 21984910 | HCID 21984910 | — |
Reaction Steps
5-(1 -Adamantyl)-4-ethyl-4H-1,2,4-triazole-3-thiol (D, Arzneim.-Forsch. 1991, 41, 1260-1264) (40 mg, 0.15 mmol) and 0.5 M methanolic NaOMe (0.3 mL, 0.15 mmol) in methanol (1 mL) was heated under reflux for 10 min. Ethyl iodide (12 μl, 0.15 mmol) was added, and the mixture was heated under reflux for 2 h. The methanol was removed in vacuo, and the residue was partitioned between CH2Cl2 and water. The organic layer was dried (MgSO4) and evaporated in vacuo. The residue was purified by chromatography on silica gel with 10% MeOH in CH2Cl2 to give 3-(1-adamantyl)-4-ethyl-5-(ethylthio)-4H-1,2,4-triazole (2), MS: 278 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07329683B2 |
| Source dataset | uspto-grants-2008_02 |
| ORD ID | ord-9eaf05275e5c427b9be2ad4dee862022 |
| Source note | uspto-grants-2008_02 |