Phosphorus oxychloride → HCID 86669008, compound

HRID 2366261Notes

Reaction equation

HRID 2366261 reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([F:8])[C:3]=1[C:9]1[S:10][C:11]2[CH:12]=[N+:13]([O-])[CH:14]=[C:15]([F:18])[C:16]=2[N:17]=1.P(Cl)(Cl)([Cl:22])=O>>[Cl:22][C:12]1[C:11]2[S:10][C:9]([C:3]3[C:4]([F:8])=[CH:5][CH:6]=[CH:7][C:2]=3[Cl:1])=[N:17][C:16]=2[C:15]([F:18])=[CH:14][N:13]=1

Participants

3

Procedure

A stirred solution of 2-(2-chloro-6-fluorophenyl)-7-fluorothiazolo[5,4-c]pyridine 5-oxide (3.0 g, 10.5 mmol) in phosphoryl chloride (50 mL) was heated at 110° C. for 45 minutes. After cooling to room temperature, the volatiles were removed under reduced pressure and the resultant residue was partitioned between a potassium carbonate saturated solution (100 mL) and EtOAc (50 mL). The aqueous phase was extracted with EtOAc (2×50 mL) and the combined organic layers were washed with water (100 mL), dried and concentrated under reduced pressure. The resultant residue was purified by column chromatography on silica gel eluting with 10% diethyl ether in pentane to afford the title compound as a colourless solid (0.71 g, 22% yield). 1H NMR (400 MHz, CDCl3): δ 8.38 (s, 1H), 7.56-7.46 (m, 1H), 7.41 (d, J=8.2 Hz, 1H), 7.21 (t, J=8.6 Hz, 1H).

Workup

  1. customthe volatiles were removed under reduced pressure
  2. customthe resultant residue was partitioned between a potassium carbonate saturated solution (100 mL) and EtOAc (50 mL)
  3. extractionThe aqueous phase was extracted with EtOAc (2×50 mL)
  4. washthe combined organic layers were washed with water (100 mL)
  5. customdried
  6. concentrationconcentrated under reduced pressure
  7. customThe resultant residue was purified by column chromatography on silica gel eluting with 10% diethyl ether in pentane

Sources & evidence

ORD record
ord-9f80d7e111724f558135d45019e85717
Source dataset
uspto-grants-2014_04
Patent number
US08697708B2

Reaction notes

Loading…