反应 #417987

ord-91deb8c4503a40b5a81d26a5843a5c7f

反应方程式

O
water
O=c1[nH]c2cc(C(F)(F)F)ccc2s1
5-trifluoromethyl-3H-benzothiazol-2-one
ClCc1cccc(-c2ncc(Br)cn2)c1
5-bromo-2-(3-chloromethylphenyl)pyrimidine
O=c1sc2ccc(C(F)(F)F)cc2n1Cc1cccc(-c2ncc(Br)cn2)c1
3-[3-(5-bromopyrimidin-2-yl)benzyl]-5-trifluoromethyl-3H-benzothiazol-2-one

溶剂

反应条件

温度
80°CELSIUS
详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    过滤the precipitate is filtered off with suction
  2. 2
    洗涤washed with methanol
  3. 3
    其他dried in vacuo
  4. 4
    其他giving beige crystals
  5. 5
    其他=3.72 min (method A)

实验过程

1 g (4.56 mmol) of 5-trifluoromethyl-3H-benzothiazol-2-one, 1.3 g (4.56 mmol) of 5-bromo-2-(3-chloromethylphenyl)pyrimidine and 4.5 g (13.69 mmol) of caesium carbonates are suspended in 15 ml of DMF and stirred at room temperature for 15 h and at 80° C. for 3 h. The suspension is added to water, and the precipitate is filtered off with suction, washed with methanol and dried in vacuo, giving beige crystals; HPLC: Rt.=3.72 min (method A);

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US08877751B2uspto-grants-2014_11