Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Iodine | HCID 807 | — |
| Reactant | Disulfide, bis(1,1-dimethylethyl) | HCID 66060 | — |
| Reactant | HCID 89668705 | HCID 89668705 | — |
| Product | HCID 117736433 | HCID 117736433 | 82% |
Reaction Steps
Di-tert-butyl disulfide (5.67 ml, 29.4 mmol) and iodine (57 mg, 0.226 mmol) were added to (2S,2'S)-di-tert-butyl 4,4′-disulfanediylbis(5-azido-2-((tert-butoxycarbonyl)amino)pentanoate) (Compound 38) (312 mg, 0.452 mmol), and the mixture was stirred at 60° C. for 18 hours. The reaction solution was purified by normal-phase silica gel column chromatography (hexane/ethyl acetate) to afford (S)-5-azido-2-tert-butoxycarbonylamino-4-tert-butyldisulfanyl-pentanoic acid tert-butyl ester (Compound 39) (161 mg, 81%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09409952B2 |
|---|
| Source dataset | uspto-grants-2016_08 |
|---|
| ORD ID | ord-e9243b885e04434ab2e5a6f7ad64fdc8 |
|---|
| Source note | uspto-grants-2016_08 |
|---|