2-Hydroxy-3-nitropyridine → 5-Amino-1-methyl[3,4'-bipyridin]-6(1H)-one

A mixture containing 10.7 g. of 1-methyl-3-nitro-5-(4-pyridinyl)-2(1H)-pyridinone and 200 ml. of dimethylformamide was warmed to dissolve the nitro-pyridinone and the solution was filtered through infusorial earth. The filtrate was charged into a 500 ml. Parr bottle with 1.2 g. of 10% palladium-on-charcoal catalyst and the mixture was shaken under 40 p.s.i. of hydrogen at room temperature for three hours, after which time no further hydrogen was taken up. The reaction mixture was filtered and the filtrate was concentrated to dryness under reduced pressure (0.1 mm.) on a water bath at 40° C. leaving 10.1 g. of brown crystalline solid. The solid was recrystallized three times from benzene-ethanol, the third time using decolorizing charcoal, to yield 4.5 g. of 3-amino-1-methyl-5-(4-pyridinyl)-2(1H)-pyridinone, m.p. 175°-176° C. after drying at room temperature in vacuo for twenty hours.

1. additionA mixture containing 10.7 g
2. filtrationthe solution was filtered through infusorial earth
3. additionThe filtrate was charged into a 500 ml
4. filtrationThe reaction mixture was filtered
5. concentrationthe filtrate was concentrated to dryness under reduced pressure (0.1 mm.) on a water bath at 40° C.
6. customleaving 10.1 g
7. customThe solid was recrystallized three times from benzene-ethanol
8. customto yield 4.5 g
9. dry with materialof 3-amino-1-methyl-5-(4-pyridinyl)-2(1H)-pyridinone, m.p. 175°-176° C. after drying at room temperature in vacuo for twenty hours

ORD record

ord-4d63bb2125534b91944ef9fbd4db83c6

Source dataset

uspto-grants-1980_04

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US04199586