Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | HCID 178462025 | HCID 178462025 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 178462026 | HCID 178462026 | 89.2% |
Reaction Steps
A solution of (2S,3R)-2-[[(2S)-6-benzyloxycarbonylamino-2-t-butoxycarbonylaminohexanoyl]amino]-3-[[(1S)-1-carboxy-2 (4-imidazolyl)ethyl]amino]butyric acid (720 mg) and 30% hydrogen bromide in acetic acid (20 ml) was sitrred for 3 hours at room temperature and the mixture was poured into ice-water (40 ml). The aqueous solution was washed with ether and subjected to a column of Dowex 50W x 8 (H+, 15 ml). The column was washed with water and the elution was carried out with 2.8% aqueous ammonia. The object fractions were collected and evaporated in vacuo. The residue was dissolved in water and lyophilized to give (2S,3R)-2-[[(2S)-2,6-diaminohexanoyl]amino]-3-[[(1S)-1-carboxy-2-(4-imidazolyl)ethyl]amino]butyric acid (399 mg) as a pale yellow powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04743614 |
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| Source dataset | uspto-grants-1988_05 |
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| ORD ID | ord-cb7c41277f844ae9bde4dc4b974e69a2 |
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| Source note | uspto-grants-1988_05 |
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