HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Carbonate → Cyclopentyl(S)-2-[(4-Aminobenzyl)-tert-butoxycarbonyl amino]-4-methylpentanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Nitrobenzyl bromide | HCID 66011 | — |
| Reactant | (S)-cyclopentyl 2-amino-4-methylpentanoate | HCID 53718217 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Cyclopentyl(S)-2-[(4-Aminobenzyl)-tert-butoxycarbonyl amino]-4-methylpentanoate | HCID 57658375 | 156.2% |
Reaction Steps
4-Nitrobenzyl bromide (11 g, 50 mmol) was dissolved in DMF (180 ml) and potassium carbonate (13.6 g, 99 mmol) added, followed by L-leucine cyclopentyl ester (Intermediate 8) (16 g, 43 mmol). The reaction was stirred for 18 h at RT. The residue was diluted with EtOAc (500 ml) and washed with water (3×100 ml), dried (Na2SO4) filtered and concentrated to dryness to give the crude product (15.8 g) which was used in the next step without further purification. LCMS purity 60%, m/z 335 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08044211B2 |
| Source dataset | uspto-grants-2011_10 |
| ORD ID | ord-e1e8bf3b6d9b4e6ea8f871bb5d406d7c |
| Source note | uspto-grants-2011_10 |