HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → L-tyrosylglycylglycyl-L-phenylalanyl-L-methionine sulfoxide hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | N-t-butoxycarbonyl-L-tyrosyl-glycylglycyl-L-phenylalanyl-L-methionine sulfoxide | HCID 22807105 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | L-tyrosylglycylglycyl-L-phenylalanyl-L-methionine sulfoxide hydrochloride | HCID 22807102 | — |
Reaction Steps
12.0 Parts N-t-butoxycarbonyl-L-tyrosylglycylglycyl-L-phenylalanyl-L-methionine sulfoxide is suspended in 100 parts by volume acetic acid and treated with 50 parts by volume 6 M HCl in dioxane. The resulting mixture is stirred at room temperature for two hours and then stripped of solvent under reduced pressure. Trituration of the residue with ether affords solid L-tyrosylglycylglycyl-L-phenylalanyl-L-methionine sulfoxide hydrochloride. This compound is represented by the following formula. ##STR6##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04144228 |
| Source dataset | uspto-grants-1979_03 |
| ORD ID | ord-838cb42d6e294829811c02d046070c7f |
| Source note | uspto-grants-1979_03 |