Triethylamine → HCID 14390313, compound

Under a nitrogen atmosphere, oxalyl chloride (2.6 g, 0.020 mole) was added dropwise (slowly) to a stirred and chilled (5°-10° C.) suspension of 2-(4-bromophenyl)-3H-imidazo[4,5-b]pyridine-3-acetic acid (6.4 g, 0.019 mole) in anhydrous dimethylformamide (50 ml). The reaction mixture was heated at 55°-60° C. for 5 hours, cooled to room temperature, and added dropwise to a stirred and chilled (10°-15° C.) suspension of N,N-dimethyl-p-phenylenediamine dihydrochloride (4.04 g, 0.0193 mole), triethylamine (8.2 g, 0.081 mole), and anhydrous dimethylformamide (100 ml). The reaction mixture was stirred overnight at room temperature, filtered, and poured into ice water (500 ml). The mixture was allowed to precipitate, and filtered. The filter cake was triturated in potassium bicarbonate solution (100 ml), filtered, and rinsed with water (100 ml). The cake was twice recrystallized from tetrahydrofuran/ethyl alcohol, giving 2.8 g (31%) of a white solid, mp 248°- 250° C.

1. temperaturechilled
2. temperatureThe reaction mixture was heated at 55°-60° C. for 5 hours
3. additionadded dropwise to
4. stirringa stirred
5. temperaturechilled
6. stirringThe reaction mixture was stirred overnight at room temperature
7. filtrationfiltered
8. additionpoured into ice water (500 ml)
9. customto precipitate
10. filtrationfiltered
11. customThe filter cake was triturated in potassium bicarbonate solution (100 ml)
12. filtrationfiltered
13. washrinsed with water (100 ml)
14. customThe cake was twice recrystallized from tetrahydrofuran/ethyl alcohol

ORD record

ord-ddafc3a365664cbca437cd5ad729d67e

Source dataset

uspto-grants-1988_09

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US04772600