HuagongsheHuagongshe Chemistry Print Report · For research reference only
Fmoc-Asp(OAll)-OH → HCID 10529786, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Fmoc-Asp(OAll)-OH | HCID 10715692 | — |
| Reactant | 2-Phenylpropan-2-yl 2,2,2-trichloroacetimidate | HCID 11140517 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 10529786 | HCID 10529786 | 93% |
Reaction Steps
2-Phenylpropan-2-yl 2,2,2-trichloroacetimidate separately synthesized by a conventional method (2.17 g, 7.74 mmol) was added to a solution of (S)-2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-4-(allyloxy)-4-oxobutanoic acid (Compound 106) (1.80 g, 4.55 mmol) in dichloromethane (40 ml), and the mixture was stirred at room temperature for 1 hour. The reaction mixture was then concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (hexane/ethyl acetate=100/0→65/35) to afford 4-allyl 1-(2-phenylpropan-2-yl) (S)-2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)succinate (Compound 107) (2.17 g, 93%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09409952B2 |
| Source dataset | uspto-grants-2016_08 |
| ORD ID | ord-6e093786928743a3b2a6901df136399a |
| Source note | uspto-grants-2016_08 |