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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1921238Generated: November 1, 2026

Triethylamine → HCID 178513362, compound

https://huagongshe.com/reaction/1921238

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantHydroxyamine hydrochlorideHCID 443297—
ReactantHCID 57992292HCID 57992292—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178513362HCID 17851336298.8%

Reaction Conditions

Temperature65 °C

Reaction Steps

517 mg 4-[5-(4-trifluoromethyl-phenyl)-2,3-dihydro-indole-1-sulfonyl]-benzonitrile were dissolved in a mixture of 10 ml tetrahydrofuran and 10 ml methanol. 1.68 g hydroxylamine hydrochloride were added followed by the addition of 3.35 ml triethylamine. The reaction mixture was stirred at 65° C. for eight hours. The solvents were removed in vacuo and the resulting residue poured into water and extracted five times with ethylacetate. The combined organic extracts were washed with brine, dried over MgSO4 and the solvent was evaporated in vacuo to obtain 550 mg N-hydroxy-4-[5-(4-trifluoromethyl-phenyl)-2,3-dihydro-indole-1-sulfonyl]-benzamidine as an oil. C22H18F3N3O3S (461,47), MS (ESI): 462.2 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08173674B2
Source datasetuspto-grants-2012_05
ORD IDord-6ac90e94ccef498183e5ec9c26f7e746
Source noteuspto-grants-2012_05