HuagongsheHuagongshe Chemistry Print Report · For research reference only
Boc-Phe(4-Cl)-N-Me-Val-N-Me-Tyr(3-tBu)-NH2 → Phe(4-Cl)-N-Me-Val-N-Me-Tyr(3-tBu)-NH2
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Boc-Phe(4-Cl)-N-Me-Val-N-Me-Tyr(3-tBu)-NH2 | HCID 131727503 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Product | Phe(4-Cl)-N-Me-Val-N-Me-Tyr(3-tBu)-NH2 | HCID 57729126 | 93.4% |
Reaction Steps
To a solution of Boc-Phe(4-Cl)-N-Me-Val-N-Me-Tyr(3-tBu)-NH2 (0.45 g, 0.697 mmol) in methylene chloride (4 ml), TFA (3 ml) was added, stirred for 20 min. and evaporated to remove the solvent under reduced pressure. The thus obtained residue was mixed with a saturated aqueous NaHCO3 solution, and extracted with methylene chloride. The organic layer was dried over anhydrous sodium 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=30:1:0.1) to give Phe(4-Cl)-N-Me-Val-N-Me-Tyr(3-tBu)-NH2 (355 mg, 93%). EI-MS:544 and 546 (M+)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07553969B1 |
| Source dataset | uspto-grants-2009_06 |
| ORD ID | ord-cfc04c07f96c458d9e4c9832ec5e1d48 |
| Source note | uspto-grants-2009_06 |