反応式
I[CH2:2][CH:3]1[S:7][CH2:6][CH:5]([S:8][C:9](=[O:11])[CH3:10])[CH2:4]1.[N-:12]=[N+:13]=[N-:14].C([N+](CCCC)(CCCC)CCCC)CCC>C(Cl)Cl>[N:12]([CH2:2][CH:3]1[S:7][CH2:6][CH:5]([S:8][C:9](=[O:11])[CH3:10])[CH2:4]1)=[N+:13]=[N-:14]参加物
4
実験手順
A solution, under argon, of 0.183 g of product from Example 140 in 1.0 ml of dry methylene chloride is treated with 0.689 g of tetra-n-butyl-ammonium azide. The reaction mixture is stirred vigorously overnight at room temperature. The reaction is concentrated in vacuo and the residue purified by chromatography (silica gel: 0-10% diethyl ether/hexane) to give 0.061 g of the desired product.
後処理
- concentrationThe reaction is concentrated in vacuo
- customthe residue purified by chromatography (silica gel: 0-10% diethyl ether/hexane)
出典と根拠
- ORDレコード
- ord-898193f0f65f4694bd51481f91ebc822
- 出典データセット
- uspto-grants-1997_04
- 特許番号
- US05623081
関連ノート
読み込み中…