HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperidine → tert-butyl[(1S)-4-[(tert-butoxycarbonyl)amino]-1-({[(2s)-2,5-diamino-5-oxopentanoyl]amino}methyl)butyl]carbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | 9h-fluoren-9-ylmethyl{(1S)-4-amino-1-[({(2s)-2,5-bis[(tert-butoxycarbonyl)amino]pentyl}amino)carbonyl]-4-oxobutyl}carbamate | HCID 70806689 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | tert-butyl[(1S)-4-[(tert-butoxycarbonyl)amino]-1-({[(2s)-2,5-diamino-5-oxopentanoyl]amino}methyl)butyl]carbamate | HCID 88986898 | — |
Reaction Steps
A solution of 33 mg (0.05 mmol) of 9H-fluoren-9-ylmethyl{(1S)-4-amino-1-[({(2S)-2,5-bis[(tert-butoxycarbonyl)amino]pentyl}amino)carbonyl]-4-oxobutyl}carbamate (Example 129A) in 1 ml of dimethylformamide is stirred after the addition of 4 mg (0.05 mmol) of piperidine at room temperature for 45 min. The solvent is evaporated and the crude product is reacted without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07446102B2 |
| Source dataset | uspto-grants-2008_11 |
| ORD ID | ord-3c17c462b843499a943ae187e63c644a |
| Source note | uspto-grants-2008_11 |