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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2227559Erstellt: 25. Oktober 2026

Phenylacetic Acid → 2-(2-Phenylacetamido)-4,5,6,7-tetrahydro-1-benzothiophene-3-carboxamide

https://huagongshe.com/reaction/2227559

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPhenylacetic AcidHCID 999—
Edukt1-HydroxybenzotriazoleHCID 75771—
Edukt2-Amino-4,5,6,7-tetrahydro-1-benzothiophene-3-carboxamideHCID 290223—
EduktHCID 178418300HCID 178418300—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelDichloromethaneHCID 6344—
Produkt2-(2-Phenylacetamido)-4,5,6,7-tetrahydro-1-benzothiophene-3-carboxamideHCID 678543—

Reaktionsbedingungen

Temperatur20 °C

Reaktionsschritte

A mixture of commercially available 2-amino-3-carbamoyl-4,5,6,7-tetrahydrobenzo[b]thiophene (5 mg, 0.026 mmol), phenylacetic acid (7 mg, 0.05 mmol), N-hydroxybenzotriazole (8.5 mg, 0.065 mmol), and N-cyclohexylcarbodiimide-N′-methylpolystyrene (loading about 1.5 mmol/g resin, 50 mg) in dichloromethane (2 ml)/dimethylformamide (0.5 ml) was agitated at 20° C. for 170 h. Afterward tris-(2-aminoethyl)-amine polystyrene (loading about 4 mmol/g resin 40 mg) was added for scavenging the hydroxybenzotriazole and the excess of acid, and the agitation was maintained for additional 24 h.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06414013B1
Quelldatensatzuspto-grants-2002_07
ORD IDord-36dc15d5abb34eac8097fefb794fa7d9
Quellennotizuspto-grants-2002_07