Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Nitrogen | HCID 947 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | HCID 67958309 | HCID 67958309 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 67958070 | HCID 67958070 | — |
Reaction Steps
In a flame dried round-bottomed flask equipped with a magnetic stir bar and under inert atmosphere (N2), a solution of (2-((4-nitro-2H-1,2,3-triazol-2-yl)methyl)thiazol-4-yl)methanol (672 mg, 2.79 mmol) in CH2Cl2 (15.0 mL) was added to a suspension of Ag2O (968 mg, 4.18 mmol) and MeI (0.52 mL, 8.36 mmol). The resulting mixture (protected form light) was stirred overnight at 40° C. The reaction mixture was filtered and the solvent was removed under reduced pressure. Purification of the residue by FC (6:4 hept-EA) gave the title compound as a yellow oil. LC-MS-conditions 07: tR=0.66 min, [M+H]+=226.27.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08846733B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-575224522f1141da9cf219ed9fddcf49 |
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| Source note | uspto-grants-2014_09 |
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