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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2211865Generated: November 1, 2026

Triethylamine → HCID 21963186, compound

https://huagongshe.com/reaction/2211865

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantBis(2-oxo-3-oxazolidinyl)phosphinic chlorideHCID 152842—
Reactant(4,5-Dimethoxy-2-nitro-phenyl)-acetic acidHCID 270941—
Reactant3-(1-Piperazinyl)-1,2-benzisothiazole monohydrochlorideHCID 11521711—
SolventDichloromethaneHCID 6344—
ProductHCID 21963186HCID 2196318671%

Reaction Steps

3-piperazin-1-yl-benzoisothiazole hydrochloride (5.29 g, 20.7 mmol) and 4,5-dimethoxy-2-nitrophenylacetic acid (5 g, 20.7 mmol) were combined in 200 mL methylene chloride with triethylamine (5.77 mL, 41.4 mmol). This solution stirred for 15 min before bis-(2-oxo-3-oxazolidinyl) phosphinic chloride (5.26 g, 20.7 mmol) was added. After stirring overnight at rt, the reaction was quenched with water and extracted into methylene chloride. The organic layer was washed with 0.5 N HCl, water, sodium bicarbonate then water before it was dried over Na2SO4 and concentrated. The residue was taken up in methylene chloride and washed with water. The organic layer was dried over sodium sulfate, and concentrated then purified by MPLC using a Biotage prepacked silica gel cartridge eluting with 3% methanol in methylene chloride to afford 6.5 g of a tan solid. Yield 71%; 100% purity at 214 nm; LCMS (APCI): 443 [M+H]+; mp 170° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07101886B2
Source datasetuspto-grants-2006_09
ORD IDord-1facc705eb7b4d08a61be48c31eacc8d
Source noteuspto-grants-2006_09