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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 43800Generated: October 29, 2026

Ethyl 3-ethynyl-6-nitro-1-benzothiophene-2-carboxylate → Ethyl 6-amino-3-ethyl-1-benzothiophene-2-carboxylate

https://huagongshe.com/reaction/43800

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 3-ethynyl-6-nitro-1-benzothiophene-2-carboxylateHCID 86648747—
ReactantHCID 178418361HCID 178418361—
CatalystHCID 178418390HCID 178418390—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 6-amino-3-ethyl-1-benzothiophene-2-carboxylateHCID 67549339—

Reaction Steps

Ethyl 3-ethynyl-6-nitro-1-benzothiophene-2-carboxylate obtained in Example (183d) was dissolved in methanol (16 mL) and THF (24 ml). A 10% palladium-carbon catalyst (120 mg) was added, and the mixture was stirred in a hydrogen atmosphere throughout the day. The reaction solution was filtered through celite and then concentrated under reduced pressure to obtain the title compound. The resulting compound was used for the next reaction without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08536197B2
Source datasetuspto-grants-2013_09
ORD IDord-8eb7df7d144a40ed91219e20f400af02
Source noteuspto-grants-2013_09