Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 178511198 | HCID 178511198 | — |
| Catalyst | Cobalt | HCID 104730 | — |
| Solvent | Ammonia methanol | HCID 21705897 | — |
| Product | Carnosine | HCID 439224 | — |
Reaction Steps
A 1-litre pressure autoclave was initial charged with 4.50 g of Raney cobalt (doped with 0.3% iron) in a mixture of 285 of conc. ammonia/methanol (m/m=1.9:1) The autoclave was closed and flushed twice with 40 bar of nitrogen and then pressurized with 45 bar of hydrogen, and the mixture was then heated to 100° C. This was followed by metering in a solution of 30.0 g (0.135 mol) of (S)-2-(cyanoacetylamino)-3-(1H-imidazol-4-yl)propionic acid (prepared according to Example 3) in a mixture of 285 g of conc. ammonia/methanol (m/m=1.9:1) over the course of one hour. After further reaction at 100° C. for one hour, the reaction mixture was cooled to room temperature. The autoclave was depressurized and the catalyst was filtered off. An in-process HPLC analysis showed that the reddish-brow-n reaction solution (310.5 g) contained 9.57% (m/m) carnosine, corresponding to a selectivity of 97% for complete conversion.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07164028B2 |
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| Source dataset | uspto-grants-2007_01 |
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| ORD ID | ord-ec6fb4fbec9e458da19b67dd71a8fc0c |
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| Source note | uspto-grants-2007_01 |
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