4,6-Dichloro-5-nitropyrimidine → 5-Amino-4,6-dichloropyrimidine

The mixture of 4,6-dichloro-5-nitropyrimidine (A-1) (20.0 g, 104 mmol) and stannous chloride dihydrate (117.7 g, 520 mmol) in EtOH (300 mL) is stirred at reflux for 2 h. The reaction mixture is allowed to cool to RT and then concentrated in vacuo. The residue is poured into ice water (300 mL) and neutralized with saturated NaHCO3 aqueous solution to adjust the pH to 5-6. The resulting mixture is stirred at RT for 30 min and then extracted with ethyl acetate (3×200 mL). The combined organic layers are washed with brine, dried over Na2SO4 and filtered. The filtrate is concentrated in vacuo to afford the product, 4,6-dichloropyrimidine-5-amine (A-2).

1. temperatureat reflux for 2 h
2. concentrationconcentrated in vacuo
3. additionThe residue is poured into ice water (300 mL)
4. stirringThe resulting mixture is stirred at RT for 30 min
5. extractionextracted with ethyl acetate (3×200 mL)
6. washThe combined organic layers are washed with brine
7. dry with materialdried over Na2SO4
8. filtrationfiltered
9. concentrationThe filtrate is concentrated in vacuo

ORD record

ord-e7dc1c2bf2974cefb952c82bba7adaf7

Source dataset

uspto-grants-2015_06

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US09056877B2