Hydrochloric Acid → HCID 178527819, compound

A solution of 2,3-diaminopyridine (10.0 g, 92 mmol), potassium hydroxide (6.8 g, 123 mmol)k, CS2 (9.4 g, 123 mmol), ethanol (100 mL), and water (20 mL) was stirred at reflux for 5 hours, then at ambient temperature overnight. Evaporation in vacuo gave a residue which was dissolved in CH2Cl2, acidified to pH 5 with 2N hydrochloric acid, and stirred for 1 hour. The resultant suspension was filtered to give 15.7 g of 2-mercaptoimidazopyridine as a brown solid. A solution of the 2-mercaptoimidazopyridine (4.23 g, 28 mmol) and geranyl chloride (4.8 g, 28 mmol) in methanol (40 mL) and 2N NaOH/H2O (40 mmol) was stirred in 16 hours at ambient temperature, evaporated, dissolved in CH2Cl2, washed with water, and dried over Na2SO4. Flash chromatography (Merck Kieselgel, 5% MeOH/CH2Cl2) gave 2.0 g (25%) of 2-[(3,7-dimethyl-2,6(E)-octadienyl)thio]-1H-imidazo[4,5-6]pyridine, 1.0 g of which was converted to its oxalate salt. m.p. 118°-121° C. NMR (DMSO-d6)δ8.20(d, J=5 Hz, 1H), 7.60(m, 2H), 5.40(d, J=7 Hz, 1H), 5.10(d, J=6 Hz, 1H), 4.00(d, J=6 Hz, 2H), 2.00(m, 4H), 1.70(s, 3H), 1.61(s, 3H), 1.60(s, 3H).

1. temperatureat reflux for 5 hours
2. customat ambient temperature
3. customovernight
4. customEvaporation in vacuo
5. customgave a residue which
6. filtrationThe resultant suspension was filtered

ORD record

ord-b6fd145fe106401d8aeab17305dcf329

Source dataset

uspto-grants-1992_04

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US05106863