HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,6-Bis(trifluoromethyl)benzoic acid → N-Benzoyl-L-valyl-L-alanyl-L-norleucine 2,6-bis (trifluoromethyl)benzoyloxy methyl ketone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,6-Bis(trifluoromethyl)benzoic acid | HCID 90618 | — |
| Reactant | Potassium Fluoride | HCID 522689 | — |
| Reactant | N-Benzoyl-L-valyl-L-alanyl-L-norleucine bromomethyl ketone | HCID 88025812 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-Benzoyl-L-valyl-L-alanyl-L-norleucine 2,6-bis (trifluoromethyl)benzoyloxy methyl ketone | HCID 86755192 | — |
Reaction Steps
A mixture of potassium fluoride (0.1 mmol, 6 mg) and 2,6-bis(trifluoromethyl)benzoic acid (0.066 mmol, 17 mg) in dry DMF (500 μl) was stirred over molecular sieves at room temperature for 5 minutes. A solution of N-benzoyl-L-valyl-L-alanyl-L-norleucine bromomethyl ketone (0.033 mmol), 16 mg) in dry DMF (500 μl) was added and the reaction mixture stirred for 1 hour. The reaction mixture was passed through a short silica plug and washed with 5% methanol in dichloromethane. Solvent was removed under vacuum and the residue purified using prep. HPLC. Freeze drying afforded (6.4 mg) as a white lyophilisate. Electrospray MS m/z 660 [MH+ ]. ##STR6##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06034066 |
| Source dataset | uspto-grants-2000_03 |
| ORD ID | ord-dc53e240f2b845d6bcf1b7375fe81ed9 |
| Source note | uspto-grants-2000_03 |