HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1482342Generated: November 1, 2026
Sodium Bicarbonate → 6-Azido-N-(tert-butoxycarbonyl)-L-norleucine
https://huagongshe.com/reaction/1482342
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Potassium bisulfate | HCID 516920 | — |
| Reactant | epsilon-tert-Butyloxycarbonyl-lysine | HCID 2733284 | — |
| Reactant | 1H-Imidazole-1-sulfonyl azide hydrochloride | HCID 23583982 | — |
| Catalyst | Copper sulfate pentahydrate | HCID 24463 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | 6-Azido-N-(tert-butoxycarbonyl)-L-norleucine | HCID 25146061 | 86% |
Reaction Steps
Sodium bicarbonate (0.65 g, 7.74 mmol) was added to a mixture of Boc-Lys-OH (Compound tk39) (1.0 g, 4.06 mmol) and copper sulfate pentahydrate (20 mg, 0.081 mmol) in methanol (15 mL)-water (3 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) (1.02 g, 4.87 mmol). Sodium bicarbonate (0.65 g, 7.74 mmol) was added to the reaction mixture, followed by stirring at room temperature for 23 hours. The reaction mixture was cooled in an ice bath, followed by addition of a saturated aqueous potassium bisulfate solution (10 mL). The resulting mixture was filtered through celite and washed with ethyl acetate, and the filtrate was then 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)-6-azido-2-((tert-butoxycarbonyl)amino)hexanoic acid (Compound tk48) (948.7 mg, 86%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09409952B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-df2565d0a9e548cf8d5dee6fa99884c3 |
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| Source note | uspto-grants-2016_08 |
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