反応 #162950

ord-199e6b45ecc84b7a80d1d68c4cc56b6c

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他The title compound was prepared
  2. 2
    その他The solid was separated
  3. 3
    ろ過filtered
  4. 4
    洗浄washed with EtOH
  5. 5
    その他dried

実験手順

The title compound was prepared by reacting 3-(3-amino-phenyl)-isoxazole-5-carboxylic acid ethyl ester with 2-chloro-6-fluoro-benzothiazole as described in Example 1, step 3. The solid was separated, filtered, washed with EtOH and dried to give the title compound in 90% yield. Mass (ES+), 384 (M++1); IR (KBr): 3423 (br), 2666 (br), 1723, 1629, 1598; 1H NMR (DMSO-d6) δ: 1.33 (t, 3H), 4.39 (q, 2H), 7.15 (m, 1H), 7.52 (m, 1H), 7.61 (m, 2H), 7.82 (s, 1H), 7.74 (m, 1H), 7.97 (m, 1H), 8.34 (m, 1H), 10.97 (br, 1H).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US08835428B2uspto-grants-2014_09