Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | O-benzyl-L-tyrosine | HCID 725701 | — |
| Reactant | Tyr(Bn)-Gly-Gly-Phe-Leu-OBn | HCID 131735616 | — |
| Product | Benzyl L-leucinate | HCID 6451313 | 88% |
Reaction Steps
On the other hand, the filtrate and the washing liquid were well washed with chlorobenzene (5 ml) and then combined with each other, thereby a clear solution was obtained. When 10% aqueous sodium carbonate solution (12 ml) was added to the solution, a solid was deposited. After the mixture was allowed to mature by stirring at room temperature for 1 hour and then under ice-cooling for 1 hour, the deposited solid was filtered, and sequentially washed with chlorobenzene (2 ml) and water (2 ml), and dried under vacuum, thereby a white solid was obtained. The purity of the target Tyr(Bn)-Gly-Gly-Phe-Leu-OBn (SEQ ID NO: 2) was 88%, and the content of Tyr(Bn) was 4.9%. Further, the crystallization yield was 88%, and the acquisition yield relative to the Leu-OBn.TsOH salt was 58%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09346850B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-755144f8cb54443fac184f06a63c6bcf |
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| Source note | uspto-grants-2016_05 |
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