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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 572317Generated: October 26, 2026

Triethylamine → HCID 25212019, compound

https://huagongshe.com/reaction/572317

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant5-(4-Methyl-5-trifluoromethyl-isoxazol-3-yl)-thiophene-2-carbonyl chlorideHCID 86628351—
Reactant1124199-11-6HCID 129319947—
Solventtetrahydrofuran N,N-dimethylformamideHCID 21974620—
ProductHCID 25212019HCID 2521201931%

Reaction Steps

A solution of dimethyl-(S)-1-piperidin-3-ylmethyl-amine, dihydrochloride (Preparative Example 29, 108 mg, 0.5 mmol) in THF/DMF (3 mL/500 μL) was treated with triethylamine (95 μL, 1.0 mmol) followed by 5-(5-Trifluoromethyl-4-methyl-isoxazol-3-yl)-thiophene-2-carbonyl chloride (74 mg, 0.25 mmol, as prepared in Example 2 Method B). The reaction mixture was vigorously stirred or 16 h then evaporated and diluted with water (5 mL). The crude reaction mixture was extracted with EtOAc (2×3 mL) which was then washed with a 1 N NaOH solution (2×3 mL), dried over MgSO4, filtered, and evaporated in vacuo to afford product as a colorless solid. The solid was dissolved in a EtOAc/hexanes (1:1) mixture (1 mL), filtered through a PTFE syringe filter, and again evaporated in vacuo to afford product as a colorless solid (31 mg, 31%). LC/MS 5.13 min, [M+1]+ 402.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09029397B2
Source datasetuspto-grants-2015_05
ORD IDord-b4c6a6304c4a41bf8ac9a27b1bec69d1
Source noteuspto-grants-2015_05