HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formaldehyde → 1,1-Dimethylethyl 2,2-dimethyl-4-({1-[4-(trifluoromethyl)phenyl]-1H-tetrazol-5-yl}methyl)-1-piperazinecarboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Azidotrimethylsilane | HCID 78378 | — |
| Reactant | 4-(Trifluoromethyl)phenyl isocyanide | HCID 2759412 | — |
| Reactant | 1,1-Dimethylethyl 2,2-dimethyl-1-piperazinecarboxylate | HCID 29922400 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 1,1-Dimethylethyl 2,2-dimethyl-4-({1-[4-(trifluoromethyl)phenyl]-1H-tetrazol-5-yl}methyl)-1-piperazinecarboxylate | HCID 68074507 | — |
Reaction Steps
To a solution of formaldehyde (0.044 mL, 0.584 mmol) in methanol (2 mL) was added 1,1-dimethylethyl 2,2-dimethyl-1-piperazinecarboxylate (125 mg, 0.584 mmol, commercially available, for example from ChemPacific Corp., Baltimore, USA). The reaction mixture was stirred at room temperature for 1 hour before the addition of 4-(trifluoromethyl)phenylisocyanide (100 mg, 0.584 mmol, Fluorochem, Old Glossop, UK) and trimethylsilyl azide (0.092 mL, 0.701 mmol). The resulting reaction mixture was stirred at room overnight.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09115132B2 |
| Source dataset | uspto-grants-2015_08 |
| ORD ID | ord-5ddbe548ed5448e39e250f8764c6066a |
| Source note | uspto-grants-2015_08 |