反应 #4375

ord-cfc067ec972b42689c43ec1a5ef3a03e

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    温度Heating
  2. 2
    其他precipitated
  3. 3
    过滤the mixture was filtered
  4. 4
    洗涤washed with acetic acid, water and acetone

实验过程

A solution of 1.12 g (0.006 mole) of 6-chlorothieno[3,2-d]pyrimidin-4(3H)-one and 15 ml of acetic acid at 80° C. was treated with 2.88 g (0.92 ml, 0.018 mole) of bromine. Heating was continued for 2.5 hours during which time solids precipitated. After cooling to room temperature, the mixture was filtered and washed with acetic acid, water and acetone. There was obtained 0.70 g (44%) of the title compound: m.p. above 280° C.; mass spectrum 264 (molecular ion and parent peak with expected isotope pattern), 239 (-27), 186 (some starting material) among others; 1H-nmr (trifluoroacetic acid) delta 7.5 ppm (starting material, s 0.1H), 9.3 (s, 1.0H). The nmr spectrum indicates that the reaction product is about 90% of the desired product; the remainder is starting material. This material is sufficiently pure for use in further reactions.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US04725599uspto-grants-1988_02