Water → HCID 21866225、化合物
反応式
[N:1]([CH2:4][C:5]1[CH:10]=[C:9]([Cl:11])[CH:8]=[CH:7][C:6]=1[C:12]1[C:16]([Cl:17])=[N:15][S:14][N:13]=1)=[N+]=[N-].O.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.[OH-].[K+]>C1COCC1.CO>[Cl:11][C:9]1[CH:8]=[CH:7][C:6]([C:12]2[C:16]([Cl:17])=[N:15][S:14][N:13]=2)=[C:5]([CH2:4][NH2:1])[CH:10]=1参加物
実験手順
To a stirred solution of 3-[2-(azidomethyl)-4-chlorophenyl]-4-chloro-1,2,5-thiadiazole (0.205 g, 0.72 mmol) and water (0.01 mL, 0.72 mmol) in THF (1.5 mL) was added triphenyl phosphine (0.188 g, 0.72 mmol). The solution was refluxed 1 h then stirred at ambient temperature for 16 h. The solution was reduced in vacuo and the residue was dissolved in MeOH. KOH (1 pellet) was added and the solution was refluxed 5 min. The solution was reduced in vacuo and partitioned between 1 M HCl and EtOAc. The aqueous phase was separated, basified with 1 M NaOH and extracted into ether. The organic phase was separated, dried (Na2SO4) and reduced in vacuo. The residue was purified by flash chromatography on silica (eluting with EtOAc/hexanes gradient, 5–10% EtOAc followed by 0.9% MeOH/0.1% NH4OH/chloroform). 1-[5-Chloro-2-(4-chloro-1,2,5-thiadiazole-3-yl)phenyl]methanamine was isolated as a yellow oil. MS m/z=260.5.
後処理
- temperatureThe solution was refluxed 1 h
- temperaturethe solution was refluxed 5 min
- custompartitioned between 1 M HCl and EtOAc
- customThe aqueous phase was separated
- extractionextracted into ether
- customThe organic phase was separated
- dry with materialdried (Na2SO4)
- customThe residue was purified by flash chromatography on silica (eluting with EtOAc/hexanes gradient, 5–10% EtOAc followed by 0.9% MeOH/0.1% NH4OH/chloroform)
出典と根拠
- ORDレコード
- ord-563f947af26b42969b779b7000f47b33
- 出典データセット
- uspto-grants-2006_12
- 特許番号
- US07144899B2
反応ノート
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