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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1514140Erstellt: 26. Oktober 2026

Triethylamine → HCID 57606122, Verbindung

https://huagongshe.com/reaction/1514140

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
Edukt(s)-(-)-Aminoquinuclidine dihydrochlorideHCID 67373739—
Edukt5-(4-Methyl-5-trifluoromethyl-isoxazol-3-yl)-thiophene-2-carbonyl chlorideHCID 86628351—
LösungsmittelDichloromethaneHCID 6344—
ProduktHCID 57606122HCID 5760612240%

Reaktionsschritte

A suspension of (S)-(−)-aminoquinuclidine dihydrochloride (55 mg, 0.275 mmol) in dichloromethane (1 mL) as treated with triethylamine (53 μL, 0.55 mmol) followed by 5-(5-Trifluoromethyl-4-methyl-isoxazol-3-yl)-thiophene-2-carbonyl chloride (74 mg, 0.25 mmol) and the reaction mixture allowed to stir for 20 hr. After this time, the reaction mixture was evaporated and the residue partitioned between EtOAc (5 mL) and a 1 N HCl solution (10 mL). The aqueous portion was then basified to pH ˜10-12 with a 1N NaOH solution. The aqueous portion was then extracted with EtOAc (10 mL) which was then washed with a brine solution (10 mL), dried over MgSO4, filtered, and evaporated in vacuo to afford product as a colorless solid (38 mg, 40%). 1H NMR (CDCl3) 1.50-1.62 (m, 1H), 1.70-1.88 (m, 3H), 2.08-2.12 (m, 2H), 2.37 (d, J=1.3, 3H), 2.72-3.10 (m, 5H), 3.44 (ddd, J=14.0, 9.7, 2.2, 1H), 4.14-4.22 (m, 1H), 6.56 (br d, J=7.0, 1H), 7.49 (d, J=4.0, 1H), 7.56 (d, J=4.0, 1H). 19F NMR −63.13. LC/MS 4.63 min, [M+1]+ 386.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08222243B2
Quelldatensatzuspto-grants-2012_07
ORD IDord-5eef000263b04b6a92f7159cdacd610f
Quellennotizuspto-grants-2012_07