HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoroacetate → HCID 178462179, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoroacetate | HCID 84468 | — |
| Reactant | Tert-butoxycarbonylalanine | HCID 85082 | — |
| Reactant | Benzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphate | HCID 151348 | — |
| Reactant | HCID 178418600 | HCID 178418600 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178462179 | HCID 178462179 | — |
Reaction Steps
443 g of trifluoroacetate of H-Arg (NO2) Leu-NH2 are dissolved in 2 l of DMF. 200 g of Boc-Ala-OH, then 500 g of BOP are added. The pH is adjusted to 7 with pH paper (on small samples of the reaction medium) with the aid of NEM. The medium is stirred and the development of the reaction is followed by TLC. The reaction is terminated after 4 hrs. The medium is evaporated to dryness in vacuo at 25°. The residue is taken up in 2 l of water and 2 l of ethyl acetate. The organic phase is washed with a 5% aqueous solution of NaHCO3, with water, dried and evaporated. The tripeptide is recrystallized in ethyl-acetate/ether, and finally dried in vacuo. It is monitored by TLC and NMR.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04704450 |
| Source dataset | uspto-grants-1987_11 |
| ORD ID | ord-be3c7ea898e04beda97c7de9a7faf593 |
| Source note | uspto-grants-1987_11 |