Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | L-Tyrosine | HCID 6057 | — |
| Reactant | Glycine methyl ester hydrochloride | HCID 122755 | — |
| Solvent | Water | HCID 962 | — |
| Product | Glycyl-L-tyrosine | HCID 92829 | — |
Reaction Steps
Gly-OMe.HCl was added to the L-Tyr-TBP prepared by converting L-Tyr into its ionic liquid form according to the method described in Example 4 such that the concentration of the former was set at a level of 1.000 mmol/kg-L-Tyr-TBP (the amount of water present in the reaction system relative to the total mass of the system: 2% by mass). Then, the mixture was stirred enough to ensure the mixture uniform. Thereafter, the mixture was heated to 37° C. or 60° C., while stirring the same in a water bath. The reaction was finished 48 hours after the initiation of the reaction, and samples, which were collected at appropriate intervals of time during the reaction, were analyzed according to the HPLC technique to confirm the formation of the intended dipeptide, i.e., L-Gly-Tyr. The results are listed in the following Table 3.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08691941B2 |
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| Source dataset | uspto-grants-2014_04 |
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| ORD ID | ord-edf2587b8a7e448db662ffc6dccd460b |
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| Source note | uspto-grants-2014_04 |
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