HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 2-(2-Amino-5-fluoroanilino)benzo[b]thiophene-3-carbonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Dithionite | HCID 24489 | — |
| Reactant | 2-(5-Fluoro-2-nitroanilino)benzo[b]thiophene-3-carbonitrile | HCID 18422243 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-(2-Amino-5-fluoroanilino)benzo[b]thiophene-3-carbonitrile | HCID 18422267 | 145.6% |
Reaction Conditions
| Temperature | 110 °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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06455521B1 |
| Source dataset | uspto-grants-2002_09 |
| ORD ID | ord-1d6f22efa0524134b2a902c64460b299 |
| Source note | uspto-grants-2002_09 |