HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 361787Generated: October 26, 2026
Ammonia → N-BOC-b-cyclohexylalanine amide
https://huagongshe.com/reaction/361787
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Isobutyl chloroformate | HCID 62365 | — |
| Reactant | (2S)-2-(((tert-butoxy)carbonyl)amino)-3-cyclohexylpropanoic acid | HCID 10588189 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | N-BOC-b-cyclohexylalanine amide | HCID 86584122 | — |
Reaction Steps
N-[N-[N-(4-(piperidin-4-yl)butanoyl)-N-ethylglycyl]aspartyl]-L-β-cyclohexyl alanine amide ##STR17##A. N-BOC-β-cyclohexylalanine (2.0 g.) and triethyl amine (1.03 ml) aredissolved together in THF (100 ml) and the solution cooled to -20° C. Isobutyl chloroformate (1.06 ml) is added and the solution stirred at -20° C. for about 30 minutes. A saturated solution of ammonia in methanol (20 ml) is added and the solution allowed to warm to room temperature and stirred at room temperature for about 18 hours. The solution is evaporated in vacuo and the residue dissolved in ethyl acetate. The ethyl acetate solution is washed with water, 5% HCl, saturated sodium bicarbonate solution, water, brine, dried over sodium sulfate, filtered and evaporated in vacuo to give N-BOC-β-cyclohexylalanine amide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05866685 |
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| Source dataset | uspto-grants-1999_02 |
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| ORD ID | ord-48ecf49b4a9a4c6eae2cd1a4652d58ff |
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| Source note | uspto-grants-1999_02 |
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