HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → tert-butyl 2-(Boc-L-methionyl)-1-hydrazine carboxylate methylsulfonium iodide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | tert-butyl 2-(Boc-L-methionyl)-1-hydrazine carboxylate | HCID 20720845 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | tert-butyl 2-(Boc-L-methionyl)-1-hydrazine carboxylate methylsulfonium iodide | HCID 20720844 | — |
Reaction Steps
A solution of the resultant tert-butyl 2-(Boc-L-methionyl)-1-hydrazine carboxylate in acetone (20 ml) was combined with methyl iodide (17 ml, 240 mmol) and stirred at room temperature overnight. The reaction mixture was concentrated, and the resultant residue was triturated from ether, collected by filtration, washed with ether and dried to obtain tert-butyl 2-(Boc-L-methionyl)-1-hydrazine carboxylate methylsulfonium iodide (19.14 g) as a colorless solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06723722B1 |
| Source dataset | uspto-grants-2004_04 |
| ORD ID | ord-6fb8d05331a14c06b9a489fd840de79d |
| Source note | uspto-grants-2004_04 |