Phosphorus oxychloride → 4,6-Dichloropyrido[3,2-d]pyrimidine

HRID 1485514Notes

Reaction equation

HRID 1485514 reaction equation
[Cl:1][C:2]1[CH:3]=[CH:4][C:5]2[NH:6][CH:7]=[N:8][C:9](=O)[C:10]=2[N:11]=1.CCN(C(C)C)C(C)C.O=P(Cl)(Cl)[Cl:24]>>[Cl:24][C:9]1[C:10]2[N:11]=[C:2]([Cl:1])[CH:3]=[CH:4][C:5]=2[N:6]=[CH:7][N:8]=1

Participants

4

Conditions

Temperature
110 °C

Procedure

To a solution of 6-chloropyrido[3,2-d]pyrimidin-4(1H)-one (150 mg, 0.83 mmol) in POCl3 (2.0 mL) was added DIPEA (0.22 mL, 1.24 mmol) at room temperature. After stirring for 1 hour at 110° C., the reaction mixture was cooled to room temperature. The reaction mixture was concentrated in vacuo, and then diluted with water and extracted with dichlormethane. The combined organic layers were washed brine, dried over anhydrous Na2SO4, filtered and concentrated in vacuo. The residue was purified by column chromatography on SiO2 (Hex:EtOAc=10:1) to give 4,6-dichloropyrido[3,2-d]pyrimidine (120 mg, 73%) as a yellow solid. 1H-NMR (CDCl3, Varian 400 MHz) δ 7.87 (1H, d, J=8.8 Hz), 8.35 (1H, d, J=8.8 Hz), 9.14 (1H, s).

Workup

  1. temperaturethe reaction mixture was cooled to room temperature
  2. concentrationThe reaction mixture was concentrated in vacuo
  3. additiondiluted with water
  4. extractionextracted with dichlormethane
  5. washThe combined organic layers were washed brine
  6. dry with materialdried over anhydrous Na2SO4
  7. filtrationfiltered
  8. concentrationconcentrated in vacuo
  9. customThe residue was purified by column chromatography on SiO2 (Hex:EtOAc=10:1)

Sources & evidence

ORD record
ord-770ad2b97421482192674867d82c2f36
Source dataset
uspto-grants-2016_08
Patent number
US09422298B2

Reaction notes

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