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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 852584Generated: October 30, 2026

Triethylamine → HCID 69357218, compound

https://huagongshe.com/reaction/852584

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantHCID 69359115HCID 69359115—
SolventEthanolHCID 702—
ProductHCID 69357218HCID 6935721855.4%

Reaction Steps

To a solution of methyl 3-{[(3-chloropropyl)sulfonyl]amino}-2-fluoro-5-nitrobenzoate (D145) (300 mg, 0.85 mmol, 1 equiv) in EtOH (30 ml) was added NEt3 (280 μl, 2 mmol, 2.3 equiv) and the resulting solution was refluxed for 1.5 h then cooled to room temperature and concentrated in vacuo. The residue was dissolved in AcOEt and the organic phase was washed with a 2N aqueous HCl solution, dried over MgSO4 and concentrated in vacuo. The residue was triturated with AcOEt/Et2O to give methyl 3-(1,1-dioxido-2-isothiazolidinyl)-2-fluoro-5-nitrobenzoate (D147) (150 mg, 55%) as a light tan solid which was used in the next step without further purification. [M+H+ NH3]+=336.3, RT=2.50 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07253198B2
Source datasetuspto-grants-2007_08
ORD IDord-22176951b3f34cb3a6653d5c4f24cde0
Source noteuspto-grants-2007_08