HuagongsheHuagongshe Chemistry Print Report · For research reference only
L-Valine → HCID 178448321, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | L-Valine | HCID 6287 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2'-(1H-Tetrazol-5-yl)-1,1'-biphenyl-4-carboxaldehyde (Losartan Impurity) | HCID 178519404 | — |
| Catalyst | Platinum | HCID 23939 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 178448321 | HCID 178448321 | — |
Reaction Steps
2′-(1H-tetrazol-5-yl)-biphenyl-4-carbaldehyde (0.79 g; 3.2 mmol) and L-Valine (0.4 g; 3.4 mmol) are suspended in 15 ml methanol. Then sodium hydroxide is added (0.27 g; 6.72 mmol) and the reaction mixture is stirred at room temperature until a clear solution is obtained. 5% Pt/C (15.8 mg; 2 wt/wt-%) is added. The autoclave is sealed and flushed with argon and hydrogen. The pressure is set to 5 bars and the reaction is stirred at 60° C. The reaction completion is monitored by HPLC. Then the autoclave is flushed with argon and the catalyst is filtered off. Further work-up and crystallisation are done similar to example 1 b2).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07943647B2 |
| Source dataset | uspto-grants-2011_05 |
| ORD ID | ord-bd173308fa2d4aa7ac708baa0cf6fc05 |
| Source note | uspto-grants-2011_05 |