HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperidine → (R)-3-(tert-butyldisulfanyl)-2-(methylamino)propanoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | Fmoc-N-methyl-S-tert-butylthio-L-cysteine | HCID 75409952 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (R)-3-(tert-butyldisulfanyl)-2-(methylamino)propanoic acid | HCID 89668411 | 45.1% |
Reaction Steps
Piperidine (1.8 ml, 18.2 mmol) was added to a solution of (R)-2-((((9H-fluoren-9-yl)methoxy)carbonyl)(methyl)amino)-3-(tert-butyldisulfanyl)propanoic acid (Compound 2c-B) (2.70 g, 6.06 mmol) in tetrahydrofuran (20 ml), and the mixture was stirred at room temperature for 30 minutes. The reaction mixture was then concentrated under reduced pressure, and the residue was purified by reverse-phase silica gel column chromatography (10 mM aqueous ammonium acetate solution/methanol=100/0→60/40) to afford (R)-3-(tert-butyldisulfanyl)-2-(methylamino)propanoic acid (Compound 2f-G) (610 mg, 45%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09409952B2 |
| Source dataset | uspto-grants-2016_08 |
| ORD ID | ord-188bde7f682d40c5a6d51dc6f665f221 |
| Source note | uspto-grants-2016_08 |