Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Nitrogen | HCID 947 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | (4-((4-Nitro-2H-1,2,3-triazol-2-yl)methyl)thiazol-2-yl)methanol | HCID 67958245 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 67957959 | HCID 67957959 | — |
Reaction Steps
In a flame dried round-bottomed flask equipped with a magnetic stir bar and under inert atmosphere (N2), a solution of (4-((4-nitro-2H-1,2,3-triazol-2-yl)methyl)thiazol-2-yl)methanol (419 mg, 1.74 mmol) in CH2Cl2 (15.0 mL) was added to a suspension of Ag2O (604 mg, 2.61 mmol) and MeI (0.33 mL, 5.21 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 (1:1 hept-EA) gave the title compound as a yellow oil. TLC: rf (1:1 hept-EA)=0.36. LC-MS-conditions 07: tR=0.68 min, [M+H]+=256.27.
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-a45a677d518a4180a3214a34addf100c |
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| Source note | uspto-grants-2014_09 |
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