HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1482360Generated: November 1, 2026
Sodium Bicarbonate → 5-Azido-N-Boc-L-Norvaline
https://huagongshe.com/reaction/1482360
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Potassium bisulfate | HCID 516920 | — |
| Reactant | (2S)-5-amino-2-{[(tert-butoxy)carbonyl]amino}pentanoic acid | HCID 7018784 | — |
| Reactant | 1H-Imidazole-1-sulfonyl azide hydrochloride | HCID 23583982 | — |
| Catalyst | Copper sulfate pentahydrate | HCID 24463 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | 5-Azido-N-Boc-L-Norvaline | HCID 23629197 | — |
Reaction Steps
Sodium bicarbonate (1.99 g, 23.68 mmol) was added to a mixture of Boc-Orn-OH (Compound tk56) (1.0 g, 4.31 mmol) and copper sulfate pentahydrate (21 mg, 0.086 mmol) in methanol (20 mL)-water (6 mL) at room temperature, followed by addition of 1H-imidazole-1-sulfonyl azide hydrochloride synthesized by the method described in the literature (Org. Lett., 2007, 9, 3797) (1.08 g, 5.17 mmol). The reaction mixture was stirred at room temperature for 24 hours. The reaction mixture was cooled in an ice bath, followed by addition of a saturated aqueous potassium bisulfate solution (8 mL). The resulting mixture was extracted with ethyl acetate (three times), and the organic phase was concentrated under reduced pressure. The resulting residue was purified by reverse-phase silica gel column chromatography (0.05% aqueous trifluoroacetic acid solution/0.05% trifluoroacetic acid-acetonitrile solution) to afford (S)-5-azido-2-((tert-butoxycarbonyl)amino)pentanoic acid (Compound tk69) (1.19 g, quant.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09409952B2 |
|---|
| Source dataset | uspto-grants-2016_08 |
|---|
| ORD ID | ord-4734c4b818814529aa0b34210d474512 |
|---|
| Source note | uspto-grants-2016_08 |
|---|