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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 649922Generated: October 27, 2026

Hydrochloric Acid → Ethyl 2-(2-amino-4-bromoanilino)benzo[b]thiophene-3-carboxylate

https://huagongshe.com/reaction/649922

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantStannous ChlorideHCID 24479—
Reactant1,4-Dibromo-2-nitrobenzeneHCID 77004—
ReactantEthyl 2-amino-1-benzothiophene-3-carboxylateHCID 699464—
ReactantEthyl 2-(4-bromo-2-nitroanilino)benzo[b]thiophene-3-carboxylateHCID 18422146—
SolventDimethyl SulfoxideHCID 679—
SolventEthanolHCID 702—
ProductEthyl 2-(2-amino-4-bromoanilino)benzo[b]thiophene-3-carboxylateHCID 18422347—

Reaction Steps

In the same manner as in Starting Material Synthesis Example 4 and using ethyl 2-aminobenzo[b]thiophene-3-carboxylate (6.0 g), 2,5-dibromonitrobenzene (8.5 g) and dimethyl sulfoxide (70 ml), crude crystals (7.3 g) of ethyl 2-(4-bromo-2-nitroanilino)benzo[b]thiophene-3-carboxylate were obtained. Without purification, in the same manner as in Starting Material Synthesis Example 21 and using ethanol (70 ml), 18% hydrochloric acid (70 ml) and tin(II) chloride.dihydrate (15.7 g), ethyl 2-(2-amino-4-bromoanilino)benzo[b]thiophene-3-carboxylate (3.3 g) was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06271225B1
Source datasetuspto-grants-2001_08
ORD IDord-d1472a7893ef471fa5e0ff186ab8c40a
Source noteuspto-grants-2001_08