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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1452565Generated: October 30, 2026

Triethylamine → HCID 57526983, compound

https://huagongshe.com/reaction/1452565

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantSodium AzideHCID 33557—
ReactantHCID 57526976HCID 57526976—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 57526983HCID 5752698399%

Reaction Conditions

Temperature0 °C

Reaction Steps

(5R)-3-[3,5-difluoro-4-(4-thiomorpholinyl)phenyl]-5-(hydroxymethyl)-oxazolidin-2-one (Intermediate 12) (15 g, 45.5 mmol) was dissolved in a mixture of triethylamine (9.6 ml, 68 mmol) and dichloromethane (200 ml). The resulting solution was cooled to 0° C. and methane sulfonyl chloride (4.6 ml, 59 mmol) was added. The reaction mixture was stirred at 0° C. for 2 hours then allowed to warm to room temperature. Water (200 ml) was added and then the organic layer separated, dried over magnesium sulfate, filtered and concentrated in vacuo. This intermediate was dissolved in dry DMF (120 ml). Sodium azide (11.8 g, 181 mmol) was added and the reaction mixture stirred at 70° C. overnight. It was diluted with dichloromethane (700 ml), washed with water (200 ml) and brine (200 ml) and dried over magnesium sulfate. Concentration in vacuo gave 16 g of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07473699B2
Source datasetuspto-grants-2009_01
ORD IDord-3ab2f15d97fb4d279134c09cb15b4ea0
Source noteuspto-grants-2009_01