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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2192283Generated: October 30, 2026

Triethylamine → HCID 178513364, compound

https://huagongshe.com/reaction/2192283

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantHydroxyamine hydrochlorideHCID 443297—
ReactantHCID 58408271HCID 58408271—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178513364HCID 178513364229%

Reaction Conditions

Temperature90 °C

Reaction Steps

223 mg 4-[5-(6-Trifluoromethyl-pyridin-3-yl)-2,3-dihydro-indole-1-sulfonyl]-benzonitrile were dissolved in a mixture of 8 ml tetrahydrofuran and 8 ml methanol. 902 mg hydroxylamine hydrochloride were added followed by the addition of 1.82 ml triethylamine. The reaction mixture was stirred at 90° C. for four hours. The solvents were removed in vacuo and the resulting residue poured into 50 ml water and extracted five times with portions of 50 ml ethylacetate. The combined organic extracts were washed with 100 ml brine, dried over MgSO4 and the solvent was evaporated in vacuo to obtain 550 mg crude N-Hydroxy-4-[5-(6-trifluoromethyl-pyridin-3-yl)-2,3-dihydro-indole-1-sulfonyl]-benzamidine. This material was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08329725B2
Source datasetuspto-grants-2012_12
ORD IDord-b5d4001992454fb791e540f4feef83c4
Source noteuspto-grants-2012_12