HuagongsheHuagongshe Chemistry Print Report · For research reference only
(R)-2-((tert-Butoxycarbonyl)amino)-3-(2,4-dichlorophenyl)propanoic acid → HCID 68432630, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (R)-2-((tert-Butoxycarbonyl)amino)-3-(2,4-dichlorophenyl)propanoic acid | HCID 7010031 | — |
| Reactant | HCID 68431420 | HCID 68431420 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | HOAt | HCID 181649 | — |
| Product | HCID 68432630 | HCID 68432630 | — |
Reaction Steps
To a mixture of 6-6 (42 mg, 0.10 mmol) and BOC-D-2,4-dichlorophenylalanine (66 mg, 2 eq) in 0.4 mL of 0.5 M HOAt in DMF and 0.5 mL of anhydrous DMF was added diisopropylcarboimide (24 mg, 2 equivalents). The reaction mixture was stirred at room temperature overnight. The solvent was evaporated in vacuo and the crude was purified with column chromatography (eluted with hexanes, ethyl acetate 1:2). The purified product, {1-(2,4-Dichloro-benzyl)-2-[2-[3-phthalimido-propyl]-4-(2-naphthalen-2-yl-ethyl)-piperazin-1-yl]-2-oxo-ethyl}-carbamic acid tert-butyl ester (6-7) was obtained as white solid, 30 mg (40%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07354923B2 |
| Source dataset | uspto-grants-2008_04 |
| ORD ID | ord-8f311a6e274f49968ba27618d8059855 |
| Source note | uspto-grants-2008_04 |