HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1620376Generated: November 1, 2026
1,5-Dibromopentane → methyl(S)-3-tert-butoxycarbonylamino-2-piperidin-1-ylpropanoate
https://huagongshe.com/reaction/1620376
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,5-Dibromopentane | HCID 8100 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | methyl (2S)-2-amino-3-{[(tert-butoxy)carbonyl]amino}propanoate hydrochloride | HCID 18334328 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | methyl(S)-3-tert-butoxycarbonylamino-2-piperidin-1-ylpropanoate | HCID 67056335 | 59.7% |
Reaction Steps
14.4 ml (104 mmol) of triethylamine are added to a solution of 8.0 g (31 mmol) of commercial methyl (S)-2-amino-3-tert-butoxycarbonylaminopropanoate hydrochloride in 160 ml of tert-butanol, and then the reaction medium is stirred for 30 min at 40° C., and filtered in order to remove the triethylammonium salts. 6 ml (44 mmol) of 1,5-dibromopentane are added to the filtrate thus obtained, and the reaction medium is heated at 80° C. for 3 days. After the insoluble material has been filtered off, the filtrate is concentrated under vacuum. The crude residue is purified by chromatography on silica gel, elution being carried out with a 70/30 heptane/ethyl acetate mixture. 5.3 g (59%) of methyl(S)-3-tert-butoxycarbonylamino-2-piperidin-1-ylpropanoate are obtained in the form of a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08772478B2 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-3ae1e6cb501e411887a921d4cbe7afb6 |
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| Source note | uspto-grants-2014_07 |
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