HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1642656Generated: November 2, 2026
Ammonia → N-(tert-butoxycarbonyl)-L-leucyl-(5R)-5-ethynyl-L-prolinamide
https://huagongshe.com/reaction/1642656
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonia | HCID 222 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | Isobutyl chloroformate | HCID 62365 | — |
| Reactant | N-(tert-butoxycarbonyl)-L-leucyl-(5R)-5-ethynyl-L-proline | HCID 71367827 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-(tert-butoxycarbonyl)-L-leucyl-(5R)-5-ethynyl-L-prolinamide | HCID 86592933 | — |
Reaction Steps
To a cold (0° C.) solution of N-(tert-butoxycarbonyl)-L-leucyl-(5R)-5-ethynyl-L-proline (2.83 mmol) and N-methyl morpholine (0.39 mL, 3.50 mmol) in THF (15 mL) was added isobutyl chloroformate (0.42 mL, 3.25 mmol). The resulting cloudy white mixture was stirred at 0° C. for 30 minutes followed by the addition of a solution of ammonia (0.5 Min dioxane, 10.0 mL, 5.0 mmol). The solution was allowed to warm to room temperature and stirred for 16 hours. The reaction mixture was diluted by the addition of 1 M HCl (100 mL), and extracted with ethyl acetate (3×100 mL). The combined organic layers were dried (sodium sulfate), filtered, and concentrated to provide the titled compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08119664B2 |
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| Source dataset | uspto-grants-2012_02 |
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| ORD ID | ord-e4dec92b07c849388ece3f70cecb05af |
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| Source note | uspto-grants-2012_02 |
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