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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1281817Generated: October 30, 2026

Water → 2-(2-Amino-5-fluoroanilino)benzo[b]thiophene-3-carbonitrile

https://huagongshe.com/reaction/1281817

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium DithioniteHCID 24489—
Reactant2-(5-Fluoro-2-nitroanilino)benzo[b]thiophene-3-carbonitrileHCID 18422243—
SolventDimethylformamideHCID 6228—
Product2-(2-Amino-5-fluoroanilino)benzo[b]thiophene-3-carbonitrileHCID 18422267145.6%

Reaction Conditions

Temperature110 °C

Reaction Steps

Sodium hydrosulfite (86%, 233 g) was suspended in dimethylformamide (240 ml) and the suspension was heated to 110° C. To this suspension was added dropwise at 110° C. a solution of 2-(5-fluoro-2-nitroanilino)benzo[b]thiophene-3-carbonitrile (120 g), dimethylformamide (720 ml) and water (27.5 ml), which solution had been heated to 65-70° C. The reaction mixture was stirred at 110° C. for 1 hour and cooled to 20° C. Water (3.3 L) was added in 6 portions over 1 hour and the mixture was stirred at 20° C. for 1.5 hours. The precipitated crystals were filtered by suction and washed with water (2 L) to give 2-(2-amino-5-fluoroanilino)benzo[b]thiophene-3-carbonitrile (158 g, (wet weight)) as ocher crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06455521B1
Source datasetuspto-grants-2002_09
ORD IDord-1d6f22efa0524134b2a902c64460b299
Source noteuspto-grants-2002_09