Hydrochloric Acid → Pyrrolo[1,2-a]pyrazine-6-carbaldehyde

Temperature

60 °C

Pyrrolo[1,2-a]pyrazine (1.92 g, 16.3 mmol) was dissolved in water (16 mL) and treated with conc. aq. HCl (4 mL, 46.4 mmol) and 37% wt aqueous formaldehyde (5.6 mL, 67 mmol). The solution was heated to 60° C. for 4 h, allowed to cool to RT and the pH adjusted to 10. The solution was extracted with EtOAc (3×50 mL) and the combined fractions dried over Na2SO4 and concentrated to dryness under vacuum. The organic residue was purified (SGC using DCM:MeOH:NH4OH eluant in 96:3:1 ratio). Recovered starting material was dissolved in water (20 mL) and conc. HCl (5 mL, 0.6 mol) and formaldehyde (7 mL, 0.9 mol). The solution was heated to 60° C. for 120 h, and then allowed to stir at RT for 240 h. The solution pH was then brought to 12 with sodium hydroxide solution (30% w/v aq) and extracted with EtOAc (4×30 mL). The organic fractions were combined, dried over Na2SO4, and concentrated to dryness under vacuum. The product was purified (SGC using DCM:MeOH:NH4OH eluant in 95:4:1 ratio) yielding the title compound (0.46 g). MS (ESI+) for m/z 149 (M+H)+. 1H NMR (CDCl3) δ 8.46 (s, 1H), 7.85 (dd,1H), 7.19 (d, 1H), 6.72 (d, 1H), 6.63 (d, 1H), 4.83 (s, 1H), 4.78 (bs,1H).

1. temperatureto cool to RT
2. extractionThe solution was extracted with EtOAc (3×50 mL)
3. dry with materialthe combined fractions dried over Na2SO4
4. concentrationconcentrated to dryness under vacuum
5. customThe organic residue was purified (SGC using DCM:MeOH:NH4OH eluant in 96:3:1 ratio)
6. customRecovered
7. dissolutionwas dissolved in water (20 mL)
8. temperatureThe solution was heated to 60° C. for 120 h
9. extractionextracted with EtOAc (4×30 mL)
10. dry with materialdried over Na2SO4
11. concentrationconcentrated to dryness under vacuum
12. customThe product was purified (SGC using DCM:MeOH:NH4OH eluant in 95:4:1 ratio)

ORD record

ord-aa888a20af6b4cf68202819307ae00e7

Source dataset

uspto-grants-2008_12

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US07462600B2