HuagongsheHuagongshe Chemistry Print Report · For research reference only
Boc-Phe(2-F)-N-Me-Val-N-Me-Tyr(3-tBu)-NH2 → Phe(2-F)-N-Me-Val-N-Me-Tyr(3-tBu)-NH2
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Boc-Phe(2-F)-N-Me-Val-N-Me-Tyr(3-tBu)-NH2 | HCID 131727505 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Product | Phe(2-F)-N-Me-Val-N-Me-Tyr(3-tBu)-NH2 | HCID 57729115 | 85% |
Reaction Steps
To a solution of Boc-Phe(2-F)-N-Me-Val-N-Me-Tyr(3-tBu)-NH2 (0.33 g, 0.525 mmol) in methylene chloride (3 ml), TFA (1.5 ml) was added, stirred for 15 min. and then evaporated to remove the solvent under reduced pressure. The residue was mixed with methylene chloride, washed with a saturated aqueous NaHCO3 solution, dried over anhydrous magnesium sulfate and evaporated to remove the solvent under reduced pressure. The thus obtained residue was subjected to silica gel column chromatography (developing solvent: chloroform:methanol:aqueous ammonia=40:1:0.1) to give Phe(2-F)-N-Me-Val-N-Me-Tyr(3-tBu)-NH2 (235 mg, 85%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07553969B1 |
| Source dataset | uspto-grants-2009_06 |
| ORD ID | ord-01509db9dce14bbea592d6646822b480 |
| Source note | uspto-grants-2009_06 |