反応 #502100

ord-72087acc94554557a02d2567ad82e1f6

反応方程式

CC1(C)OB(c2ccc(N)nc2)OC1(C)C
5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-ylamine
CCOC(=O)CBr
ethyl 2-bromoacetate
Br.CCOC(=O)Cn1cc(B2OC(C)(C)C(C)(C)O2)ccc1=N
compound
Br.CCOC(=O)Cn1cc(B2OC(C)(C)C(C)(C)O2)ccc1=N
Ethyl[2-imino-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2H-pyridin-1-yl]acetate hydrobromide

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    ろ過A precipitate forms, and is recovered by filtration
  2. 2
    洗浄washed with diethyl ether
  3. 3
    乾燥with ethanol, and oven-dried under reduced pressure

実験手順

5.0 g of 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-ylamine in 7.6 ml of ethyl 2-bromoacetate are placed in a round-bottomed flask and the mixture is stirred at ambient temperature for 20 h. A precipitate forms, and is recovered by filtration, washed with diethyl ether and then with ethanol, and oven-dried under reduced pressure. 8.78 g of compound are obtained.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US08088765B2uspto-grants-2012_01