Phosphorus oxychloride → HCID 59215154, compound

HRID 2252309Notes

Reaction equation

HRID 2252309 reaction equation
O=P(Cl)(Cl)[Cl:3].[CH3:6][O:7][C:8]1[CH:13]=[CH:12][C:11]([C:14]2[N:15]=[C:16](O)[C:17]3[CH:18]=[CH:19][C:20]([C:24]([F:27])([F:26])[F:25])=[N:21][C:22]=3[CH:23]=2)=[CH:10][CH:9]=1>>[Cl:3][C:16]1[N:15]=[C:14]([C:11]2[CH:12]=[CH:13][C:8]([O:7][CH3:6])=[CH:9][CH:10]=2)[CH:23]=[C:22]2[C:17]=1[CH:18]=[CH:19][C:20]([C:24]([F:27])([F:26])[F:25])=[N:21]2

Participants

3

Conditions

Temperature
100 °C

Procedure

POCl3 (3 mL) was added to 7-(4-methoxyphenyl)-2-trifluoromethyl-[1,6]naphthyridin-5-ol (Example 19) (125 mg, 0.4 mmol). The mixture was heated at 100° C. for 3 hours. The excess POCl3 was concentrated under reduced pressure. The residue was diluted with CH2Cl2, washed with sat. NaHCO3, dried over Na2SO4, and concentrated giving the title compound (73 mg, 55%) as an orange solid.

Workup

  1. concentrationThe excess POCl3 was concentrated under reduced pressure
  2. additionThe residue was diluted with CH2Cl2
  3. washwashed with sat. NaHCO3
  4. dry with materialdried over Na2SO4
  5. concentrationconcentrated

Sources & evidence

ORD record
ord-561613fb86264cd58d4a4cb3cc7aee01
Source dataset
uspto-grants-2008_01
Patent number
US07321041B2

Reaction notes

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