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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 385696Generated: October 29, 2026

Benzyl[3-(aminocarbonyl)-5-(2,4-difluorophenyl)-2-thienyl]carbamate → 2-Amino-5-(2,4-difluorophenyl)thiophene-3-carboxamide

https://huagongshe.com/reaction/385696

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl[3-(aminocarbonyl)-5-(2,4-difluorophenyl)-2-thienyl]carbamateHCID 59526381—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product2-Amino-5-(2,4-difluorophenyl)thiophene-3-carboxamideHCID 59526295—

Reaction Steps

A suspension of benzyl[3-(aminocarbonyl)-5-(2,4-difluorophenyl)-2-thienyl]carbamate (240 mg, 0.618 mmol) and 10% palladium on carbon (326 mg, 0.306 mmol) in ethanol (130 mL) was placed under a hydrogen atmosphere by performing 5×15 second vacuum/hydrogen purge (supplied by balloon) fill cycles while vigorously stirring the mixture. The reaction was heated to reflux for 18 hours and then allowed to cool to ambient temperature. The suspension was filtered; the filtrate was collected and concentrated to yield the title compound as a light yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367706B2
Source datasetuspto-grants-2013_02
ORD IDord-95a6580003ba427292fd01887558f7da
Source noteuspto-grants-2013_02