Hydrazine hydrate (1:1) → Ethyl acetate methanol ammonium hydroxide

Temperature

55 °C

2-[4-(Cyanomethyl)phenyl]-3-[4-[2-(1-pyrrolidinyl)ethoxy]benzyl]benzo[b]thiophene (1.39 g) was dissolved in ethanol and warmed to 55° C. before it was treated with Raney nickel (1 mL slurry in water) followed by addition of hydrazine monohydrate (1.5 mL). The resulting mixture was allowed to stir at 55° C. for 30 min or until the evolution of gas had stopped. The cooled reaction mixture was filtered through diatomaceous earth, rinsed with methanol and dichloromethane. The filtrate was diluted with saturated sodium bicarbonate (50 mL) and extracted with dichloromethane (50 mL×3). The combined organic layers were dried with sodium sulfate and concentrated. Chromatography with NH4OH:MeOH:EtOAc (5:10:85) afforded the product (1.30 g)

1. customThe cooled reaction mixture
2. filtrationwas filtered through diatomaceous earth
3. washrinsed with methanol and dichloromethane
4. additionThe filtrate was diluted with saturated sodium bicarbonate (50 mL)
5. extractionextracted with dichloromethane (50 mL×3)
6. dry with materialThe combined organic layers were dried with sodium sulfate
7. concentrationconcentrated

ORD record

ord-e94a51b0edef4a2f99e6650d0d8f127f

Source dataset

uspto-grants-2002_05

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US06391901B1