HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dicyclohexylcarbodiimide → BocPro-Phe-MePhe-Gly-Leu-MetNH2
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | N-Hydroxysuccinimide | HCID 80170 | — |
| Reactant | BocPro-Phe-MePhe-GlyOH | HCID 131713702 | — |
| Reactant | HLeu-MetNH2 hydrochloride | HCID 131713703 | — |
| Product | BocPro-Phe-MePhe-Gly-Leu-MetNH2 | HCID 131713701 | 100% |
Reaction Steps
Condensation of BocPro-Phe-MePhe-GlyOH (0.76 g.) and HLeu-MetNH2 hydrochloride salt (Example 1, 0.39 g.) using dicyclohexylcarbodiimide and N-hydroxysuccinimide gave BocPro-Phe-MePhe-Gly-Leu-MetNH2 in 100% yield. De-t-butoxycarbonylation of BocPro-Phe-MePhe-Gly-Leu-MetNH2 (1.07 g.) using hydrogen chloride in acetic acid gave HPro-Phe-MePhe-Gly-Leu-MetNH2, which was isolated as the amorphous white solid phosphate (1:1) salt dihydrate in 22% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04472305 |
| Source dataset | uspto-grants-1984_09 |
| ORD ID | ord-715fe5a9b14646dc8ec12ffb084b5fe9 |
| Source note | uspto-grants-1984_09 |