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

HRID 2369392Notes

Reaction equation

HRID 2369392 reaction equation
P(Cl)(Cl)([Cl:3])=O.[CH2:6]([C:8]1[S:17][C:11]2[N:12]=[CH:13][N:14]=[C:15](O)[C:10]=2[CH:9]=1)[CH3:7]>O1CCOCC1>[Cl:3][C:15]1[C:10]2[CH:9]=[C:8]([CH2:6][CH3:7])[S:17][C:11]=2[N:12]=[CH:13][N:14]=1

Participants

4

Procedure

Phosphoryl trichloride (2.3 mL, 3.00 equiv) was added to a solution of 6-ethylthieno[2,3-d]pyrimidin-4-ol (1.5 g, 8.32 mmol, 1.00 equiv) in dioxane (15 mL) dropwise with stirring at room temperature. The resulting solution was stirred overnight at 110° C. in an oil bath. The resulting solution was cooled and quenched by the addition of 100 mL of water and ice mixture. The resulting solution was extracted with 3×100 mL of ethyl acetate and the organic layers combined. The resulting mixture was washed with 3×200 mL of brine. The mixture was dried over anhydrous sodium sulfate and concentrated under vacuum. The residue was applied onto a silica gel column with ethyl acetate/petroleum ether (1/10) to yield 700 mg (42%) of 4-chloro-6-ethylthieno[2,3-d]pyrimidine as a yellow solid. MS: m/z 199 (M+H)+.

Workup

  1. stirringThe resulting solution was stirred overnight at 110° C. in an oil bath
  2. temperatureThe resulting solution was cooled
  3. customquenched by the addition of 100 mL of water and ice mixture
  4. extractionThe resulting solution was extracted with 3×100 mL of ethyl acetate
  5. washThe resulting mixture was washed with 3×200 mL of brine
  6. dry with materialThe mixture was dried over anhydrous sodium sulfate
  7. concentrationconcentrated under vacuum

Sources & evidence

ORD record
ord-2e6c6eefed23496d9360ea1afc9ee2fa
Source dataset
uspto-grants-2014_04
Patent number
US08703941B2

Reaction notes

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