反応 #45429

ord-fabe84145ad840b4b3c077c5acb259a2

反応方程式

Nc1ncc(CO)c2scc(Br)c12
solution
Nc1ncc(CO)c2scc(Br)c12
(4-amino-3-bromothieno[3,2-c]pyridin-7-yl)methanol
Nc1ncc(C=O)c2scc(Br)c12
desired product
収率 89.0%
Nc1ncc(C=O)c2scc(Br)c12
4-amino-3-bromothieno[3,2-c]pyridine-7-carbaldehyde
収率 89.0%

溶媒

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    ろ過filtered through diatomaceous earth (Celite®)
  2. 2
    洗浄The pad was washed with THF and dichloromethane
  3. 3
    濃縮the combined filtrates were concentrated

実験手順

A solution of Example 277E (1 g, 3.86 mmol) in THF (100 mL) was treated with MnO2 (2.66 g, 42.1 mmol), stirred overnight at room temperature, and filtered through diatomaceous earth (Celite®). The pad was washed with THF and dichloromethane and the combined filtrates were concentrated to provide 0.88 g (89% yield) of the desired product. MS (ESI(+)) m/e 256.8, 258.8 (M+H)+.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US07737160B2uspto-grants-2010_06