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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1909095Generated: October 31, 2026

tert-Butyl acetate → Delamanid

https://huagongshe.com/reaction/1909095

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl acetateHCID 10908—
ReactantSodium HydroxideHCID 14798—
ReactantSodium AcetateHCID 517045—
Reactant(R)-1-[4-(2,3-epoxy-2-methylpropoxy)phenyl]-4-[4-(trifluoromethoxy)phenoxy]piperidineHCID 25121191—
ReactantHCID 178526855HCID 178526855—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductDelamanidHCID 648046673.7%

Reaction Conditions

Temperature100 °C

Reaction Steps

(R)-1-[4-(2,3-epoxy-2-methylpropoxy)phenyl]-4-[4-(trifluoromethoxy)phenoxy]piperidine (10.0 g, 23.6 mmol, optical purity of 94.3% ee), 2-chloro-4-nitroimidazole (4.0 g, 27.2 mmol), sodium acetate (0.4 g, 4.9 mmol), and t-butyl acetate (10 ml) were mixed and stirred at 100° C. for 3.5 hours. Methanol (70 ml) was added to the reaction mixture, and then a 25% sodium hydroxide aqueous solution (6.3 g, 39.4 mmol) was added thereto dropwise while cooling with ice. The resulting mixture was stirred at 0° C. for 1.5 hours, and further stirred at approximately room temperature for 40 minutes. Water (15 ml) and ethyl acetate (5 ml) were added thereto, and the mixture was stirred at 45 to 55° C. for 1 hour. The mixture was cooled to room temperature, and the precipitated crystals were collected by filtration. The precipitated crystals were subsequently washed with methanol (30 ml) and water (40 ml). Methanol (100 ml) was added to the resulting crystals, followed by stirring under reflux for 30 minutes. The mixture was cooled to room temperature. The crystals were then collected by filtration and washed with methanol (30 ml). The resulting crystals were dried under reduced pressure, obtaining 9.3 g of the objective product (yield: 73%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08598358B2
Source datasetuspto-grants-2013_12
ORD IDord-e922d4f9b0074e83bface9585c9b6862
Source noteuspto-grants-2013_12