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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
ReactantPotassium bisulfateHCID 516920—
Reactantepsilon-tert-Butyloxycarbonyl-lysineHCID 2733284—
Reactant1H-Imidazole-1-sulfonyl azide hydrochlorideHCID 23583982—
CatalystCopper sulfate pentahydrateHCID 24463—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product6-Azido-N-(tert-butoxycarbonyl)-L-norleucineHCID 2514606186%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09409952B2
Source datasetuspto-grants-2016_08
ORD IDord-df2565d0a9e548cf8d5dee6fa99884c3
Source noteuspto-grants-2016_08