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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2227559Generated: October 25, 2026

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

https://huagongshe.com/reaction/2227559

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylacetic AcidHCID 999—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant2-Amino-4,5,6,7-tetrahydro-1-benzothiophene-3-carboxamideHCID 290223—
ReactantHCID 178418300HCID 178418300—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product2-(2-Phenylacetamido)-4,5,6,7-tetrahydro-1-benzothiophene-3-carboxamideHCID 678543—

Reaction Conditions

Temperature20 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06414013B1
Source datasetuspto-grants-2002_07
ORD IDord-36dc15d5abb34eac8097fefb794fa7d9
Source noteuspto-grants-2002_07