HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 475338Generated: October 30, 2026
Ammonia → N-(tert-butoxycarbonyl)-L-leucyl-(5R)-5-ethynyl-L-prolinamide
https://huagongshe.com/reaction/475338
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 M in 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 | US08637546B2 |
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| Source dataset | uspto-grants-2014_01 |
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| ORD ID | ord-7188a4212ca048b882b5c2a78c7f134d |
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| Source note | uspto-grants-2014_01 |
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