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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1955120Generated: November 3, 2026

Ammonium Chloride → (S)-N-[[3-[3-Fluoro-4-[3-(3-hydroxypropyl)-1H-pyrrol-1-yl]phenyl]-2-oxo-5-oxazolidinyl]methyl]acetamide

https://huagongshe.com/reaction/1955120

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantLithium borohydrideHCID 4148881—
ReactantHCID 10740673HCID 10740673—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product(S)-N-[[3-[3-Fluoro-4-[3-(3-hydroxypropyl)-1H-pyrrol-1-yl]phenyl]-2-oxo-5-oxazolidinyl]methyl]acetamideHCID 1069086839%

Reaction Steps

A solution of 275 mg(0.66 mmol) of the compound of Example 24 in 15 mL THF was treated with 287 mg(13.2 mmol) of lithium borohydride followed by stirring at ambient temperature for 18 h. The solution was treated with lmL of saturated ammonium chloride solution, diluted with ethyl acetate, and extracted with water (3×). Drying (Na2SO4) and concentration in vacuo afforded an oil, which was chromatographed over 20 g of 230-400 mesh silica gel eluting with 2-4%(v/v) methanol in dichloromethane. These procedures afforded 96 mg(39%) of the title compound as a white solid. 1H NMR (CDCl3) δ7.74, 7.66, 7.38, 7.27, 7.18, 6.95, 6.61, 5.98, 4.82, 4.37, 4.27, 4.09, 3.83, 3.68, 2.88, 2.82, 2.62, 2.04, 1.79.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06124334
Source datasetuspto-grants-2000_09
ORD IDord-74ff729c886442b1bb64e7b136718182
Source noteuspto-grants-2000_09