Thionyl Chloride → HCID 178478890, compound

A slurry of 40 mg (0.35 mmol) of 4-imidazolecarboxylic acid in 5 mL of dichloroethane was treated with 1 drop DMF followed by 0.10 mL (1.37 mmol) of SOCl2. The mixture was heated to mild reflux for 2 h, concentrated in vacuo, and the residue reconstituted in 5 mL dichloroethane. A solution of 300 mg (0.70 mmol) of 2-(4-aminophenyl)-3-[4-[2-(1-pyrrolidinyl)ethoxy]benzyl]benzo[b]thiophene (Part D) in 5 mL of dichloroethane was added and the mixture heated to mild reflux for 16 h. The reaction was diluted with 10 mL of sat'd aq NaHCO3, the two layers were separated, and the aqueous layer extracted with CHCl3 (3×10 mL). The combined organic layers were dried (K2CO3), filtered and concentrated in vacuo. Radial chromatography (SiO2; 2% then 4% then 5% MeOH in CHCl3 sat'd with NH4OH) afforded 90 mg (0.17 mmol; 49%) of the free base of the title compound as a solid. The product was taken up in 2 mL of H2O and was treated with 1 mL of 1 N aq HCl. The solution was lyophilized to give the title compound.

1. temperatureThe mixture was heated
2. temperatureto mild reflux for 2 h
3. concentrationconcentrated in vacuo
4. temperaturethe mixture heated
5. temperatureto mild reflux for 16 h
6. customthe two layers were separated
7. extractionthe aqueous layer extracted with CHCl3 (3×10 mL)
8. dry with materialThe combined organic layers were dried (K2CO3)
9. filtrationfiltered
10. concentrationconcentrated in vacuo

ORD record

ord-10ea9916ca8d4921b9ff490b7ddb1754

Source dataset

uspto-grants-2002_05

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US06391901B1