HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → Boc-Phe(4-F)-N-Me-Val-Tyr(3-tBu)-NH2
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | N-(tert-Butoxycarbonyl)-4-fluoro-L-phenylalanine | HCID 7020910 | — |
| Reactant | N-Me-Val-Tyr(3-tBu)-NH2 | HCID 131722732 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Boc-Phe(4-F)-N-Me-Val-Tyr(3-tBu)-NH2 | HCID 131727517 | 85.3% |
Reaction Steps
To a solution of Boc-Phe(4-F)-OH (890 mg, 3.14 mmol), N-Me-Val-Tyr(3-tBu)-NH2 (1 g, 2.86 mmol) and CMPI (804 mg, 3.15 mmol) in THF (20 ml), TEA (1.2 ml, 7.16 mmol) was added under cooling with ice and stirred at room temperature overnight. The reaction mixture was mixed with water and extracted with ethyl acetate. The organic layer was washed with saturated brine, 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: acetone:n-hexane=1:2), giving Boc-Phe(4-F)-N-Me-Val-Tyr(3-tBu)-NH2 (1.5 g, 85%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07553969B1 |
| Source dataset | uspto-grants-2009_06 |
| ORD ID | ord-cfec7b9633704949818a79d50552537e |
| Source note | uspto-grants-2009_06 |