HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 525004Generated: October 31, 2026
(S)-2-((tert)-Butoxycarbonyl)amino)butanoic acid → HCID 86722024, compound
https://huagongshe.com/reaction/525004
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | (S)-2-((tert)-Butoxycarbonyl)amino)butanoic acid | HCID 2755934 | — |
| Reactant | HCID 86722025 | HCID 86722025 | — |
| Solvent | Diisopropyl Ether | HCID 7914 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 86722024 | HCID 86722024 | 59.7% |
Reaction Steps
1.60 g (6.18 mmol) of 1-amino-N-(3,5-difluorophenyl)-1H-imidazole-2-carboxamide, 1.64 g (8.65 mmol) of (S)-2-(tert-butoxycarbonylamino)butanoic acid and 1.34 g (8.65 mmol) of EDCHCl were dissolved in 45 mL of THF and stirred at 55° C. overnight and at room temperature for 2 days. Then the solvent was evaporated and the crude residue was taken up in ethyl acetate and washed with brine. The organic layer was dried over magnesium sulphate, filtered and the solvent was evaporated. The solid obtained was redissolved in the minimum amount of ethyl acetate and diisopropylether was added until a solid precipitated, which was filtered to furnish 1.51 g (57% yield) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09340547B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-37171a4adfef4076abf254a03be6212d |
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| Source note | uspto-grants-2016_05 |
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