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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 723823Generated: October 31, 2026

O-Methylhydroxylamine hydrochloride → HCID 9881022, compound

https://huagongshe.com/reaction/723823

Reaction equation

Participants

RoleNameHCIDCharge
ReactantO-Methylhydroxylamine hydrochlorideHCID 521874—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantHCID 23730106HCID 23730106—
SolventWaterHCID 962—
SolventOxolane--water (1/1)HCID 21881883—
ProductHCID 9881022HCID 9881022—

Reaction Steps

A mixture of (5R)-(−)-3-[3-fluoro-4-(4-morpholinyl)phenyl]-2-oxo-5-oxazolidinecarboxylic acid (EXAMPLE 1, Step 1, 150 mg, 0.483 mmol) and O-methylhydroxylamine hydrochloride (61 mg, 0.724 mmol) in tetrahydrofuran/water (1/1, 4.8 mL) is treated with 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (278 mg, 1.45 mmol), and the resulting mixture is stirred at ambient temperature for 30 minutes and is then diluted with water (10 mL) and extracted with ethyl acetate (2×20 mL). The combined organic phase is washed with water (10 mL) and saline (10 mL), dried over anhydrous sodium sulfate and concentrated under reduced pressure, and the crude product is chromatographed on a Flash 40S silica gel (40 g, 32–63 μm) cartridge, eluting with methanol/methylene chloride (2.5/97.5). Pooling and concentration of those fractions with an Rf=0.53 by TLC (methanol/chloroform, 10/90) gives the title compound, mp 206–208° C. (decomp.); MS (ESI+) for C51H18FN3O5 m/z 340 (M+H)+; [α]25D=−56° (c 0.92, DMSO).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07141588B2
Source datasetuspto-grants-2006_11
ORD IDord-f0073dff6dd2404a9a30550836f55118
Source noteuspto-grants-2006_11