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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2360994Generated: November 1, 2026

Water → Ethyl (1S,3R,4S)-4-azido-3-[(tert-butoxycarbonyl)amino]cyclohexane-1-carboxylate

https://huagongshe.com/reaction/2360994

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantEthyl AcetateHCID 8857—
ReactantSodium AzideHCID 33557—
ReactantEthyl (1S,3R,4R)-3-[[(1,1-dimethylethoxy)carbonyl]amino]-4-[(methylsulfonyl)oxy]cyclohexanecarboxylateHCID 86593060—
CatalystTetramethylammonium chlorideHCID 6379—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductEthyl (1S,3R,4S)-4-azido-3-[(tert-butoxycarbonyl)amino]cyclohexane-1-carboxylateHCID 57416168—

Reaction Conditions

Temperature60 °C

Reaction Steps

Sodium azide (357.6 mg) and tetramethylammonium chloride (91.0 mg) were added at room temperature to a solution (2 mL) of ethyl (1S,3R,4R)-3-[(t-butoxycarbonyl)amino]-4-methanesulfonyloxycyclohexanecarboxylate (1.01 g) in N-methyl-2-pyrrolidone, followed by stirred at 60° C. for 74 hours. Water and ethyl acetate were added to the reaction mixture, and the organic layer was washed with aqueous saturated sodium bicarbonate solution and water, followed by drying over magnesium sulfate anhydrate. The solvent was evaporated under reduced pressure, and the residue was subjected to silica gel column chromatography (n-hexane:ethyl acetate=4:1), to thereby yield 648.3 mg of the title compound. Spectral data of this compound were found to be identical with those of the compound of Example 5.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08686189B2
Source datasetuspto-grants-2014_04
ORD IDord-78d37fe6c10642f0a45635be8641753d
Source noteuspto-grants-2014_04