반응 #1583811

ord-d76d40b15ec047a1847095d36fc3b594

반응 방정식

O=C1CCC(=O)N1Br
N-bromosuccinimide
CCc1nc(-c2ccc(F)cc2)cs1
2-ethyl-4-(4-fluorophenyl)-1,3-thiazole
O
water
CCc1nc(-c2ccc(F)cc2)c(Br)s1
5-Bromo-2-ethyl-4-(4-fluorophenyl)-1,3-thiazole

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타the organic phase is separated off
  2. 2
    세척washed with saturated NHCO3 solution
  3. 3
    건조dried over MgSO4
  4. 4
    농축concentrated under reduced pressure

실험 절차

At room temperature, 1.72 g (9.64 mmol) of N-bromosuccinimide are added a little at a time to a solution of 2.00 g (9.64 mmol) of 2-ethyl-4-(4-fluorophenyl)-1,3-thiazole in 40 ml of dichloromethane. After 2 h, 50 ml of water are added to the reaction mixture, and the organic phase is separated off, washed with saturated NHCO3 solution, dried over MgSO4 and concentrated under reduced pressure. This gives 2.47 g (85%) of the desired product; 1H-NMR(DMSO-d6) δ: 7.92 (m, 2H), 7.32 (m, 2H), 3.02 (q, 2H), 1.31 (t, 3H).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US09198426B2uspto-grants-2015_12