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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 747193Generated: October 30, 2026

Sodium Chloride → 5-Azidomethyl-3-(5-bromo-pyridin-2-yl)-4,5-dihydro-isoxazole

https://huagongshe.com/reaction/747193

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ChlorideHCID 5234—
ReactantSodium AzideHCID 33557—
ReactantMethanesulfonic acid 3-(5-bromo-pyridin-2-yl)-4,5-dihydro-isoxazol-5-ylmethyl esterHCID 59749444—
SolventDimethylformamideHCID 6228—
Product5-Azidomethyl-3-(5-bromo-pyridin-2-yl)-4,5-dihydro-isoxazoleHCID 1795446958.6%

Reaction Conditions

Temperature75 °C

Reaction Steps

Methanesulfonic acid 3-(5-bromo-pyridin-2-yl)-4,5-dihydro-isoxazol-5-ylmethyl ester (30.5 g, 90.77 mmol) was added to dimethyl formamide (50 ml) followed by addition of sodium azide (11.8 g, 181.5 mmol). The mixture was heated to 75° C. for five hours and then added to aqueous sodium chloride (100 ml) followed by extraction with ethyl acetate (3×200 ml). The organic layers were combined, dried over sodium sulfate, and concentrated in vacuo to yield the desired product (15 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07396847B2
Source datasetuspto-grants-2008_07
ORD IDord-61406d142970422e9faea61043c10f5b
Source noteuspto-grants-2008_07