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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1740809Erstellt: 27. Oktober 2026

Triethylamine → 1-[3-[(2-Dimethylaminoethyl)methylcarbamoyl]phenylcarbamoyl]-5-methylthio-6-trifluoromethyl indoline

https://huagongshe.com/reaction/1740809

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktOxalyl chlorideHCID 65578—
Edukt1,2-Ethanediamine, N1,N1,N2-trimethyl-HCID 67338—
Edukt5-Methylthio-6-trifluoromethyl-1-(3-carboxy Phenyl Carbamoyl)indolineHCID 18005107—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelDichloromethaneHCID 6344—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt1-[3-[(2-Dimethylaminoethyl)methylcarbamoyl]phenylcarbamoyl]-5-methylthio-6-trifluoromethyl indolineHCID 5413766383,2%

Reaktionsschritte

The carboxylic acid from Example 12 (0.5 g, 1.25 mmol) in dichloromethane (10 ml) was treated with oxalyl chloride (0.3 ml, 3.4 mol) and DMF (catalytic). Solution was stirred for 1 h and evaporated to dryness. The residue in dry THF (5 ml) was added to a stirred solution of triethylamine (0.3 ml, 4 mmol) and N,N,N'-trimethylethylenediamine (0.5 ml, 4.5 mmol) in dry THF (10 ml). Following 3 hours at room temperature, the solution was partitioned (H2O/EtOAc). Drying and removal of the organic layers followed by recrystallisation (EtOAc/60°-80° petrol) afforded the title compound (0.5 g, 83%) as a white solid. M.pt. 140°-141° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05972937
Quelldatensatzuspto-grants-1999_10
ORD IDord-358a48d0a59041da99095b831ed2776a
Quellennotizuspto-grants-1999_10