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
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Phenylacetic Acid | HCID 999 | — |
| Edukt | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Edukt | 2-Amino-4,5,6,7-tetrahydro-1-benzothiophene-3-carboxamide | HCID 290223 | — |
| Edukt | HCID 178418300 | HCID 178418300 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | 2-(2-Phenylacetamido)-4,5,6,7-tetrahydro-1-benzothiophene-3-carboxamide | HCID 678543 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06414013B1 |
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| Quelldatensatz | uspto-grants-2002_07 |
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| ORD ID | ord-36dc15d5abb34eac8097fefb794fa7d9 |
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| Quellennotiz | uspto-grants-2002_07 |
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