반응 #2298626

ord-34e2d7db353e435aa16e02584e3844b6

반응 방정식

O=c1[nH]cnc2cc(-c3ccsc3)sc12
6-(3-thienyl)-3H-thieno[3,2-d]pyrimid-4-one
O=c1[nH]cnc2cc(-c3ccsc3)sc12
6-(3-Thienyl)-3H-thieno[3,2-d]pyrimid-4-one
O=P(Cl)(Cl)Cl
phosphorus oxychloride
O=C([O-])O.[Na+]
sodium bicarbonate
Clc1ncnc2cc(-c3ccsc3)sc12
6-(3-thienyl)-4-chlorothieno[3,2-d]pyrimidine
수율 81.0%

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도at reflux for 1 hour
  2. 2
    추출extracted with ethyl acetate
  3. 3
    세척The organic layer was washed with water
  4. 4
    건조dried over anhydrous magnesium sulfate
  5. 5
    기타the solvent evaporated under reduced pressure

실험 절차

A solution of 6-(3-thienyl)-3H-thieno[3,2-d]pyrimid-4-one (218, 74 mg, 0.32 mmol) in phosphorus oxychloride (2 mL) under N2 was heated at reflux for 1 hour. The resulting solution was allowed to cool to room temperature, poured into a saturated aqueous solution of sodium bicarbonate to neutralize and then extracted with ethyl acetate. The organic layer was washed with water followed by saturated aqueous sodium chloride, dried over anhydrous magnesium sulfate and the solvent evaporated under reduced pressure to yield 6-(3-thienyl)-4-chlorothieno[3,2-d]pyrimidine (65 mg, 81% yield) as a yellow solid.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: USRE039267E1uspto-grants-2006_09