反応 #2467966

ord-366344c268d847cd918ad0954929283f

反応方程式

O
water
[NH4+].[OH-]
ammonium hydroxide
COC(=O)c1sc([N+](=O)[O-])cc1N=NN(C)C
methyl 3-[(dimethylamino)diazenyl]-5-nitrothiophene-2-carboxylate
CN(C)N=Nc1cc([N+](=O)[O-])sc1C(N)=O
solid
収率 26.0%
CN(C)N=Nc1cc([N+](=O)[O-])sc1C(N)=O
3-[(Dimethylamino)diazenyl]-5-nitrothiophene-2-carboxamide
収率 26.0%

溶媒

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    workup.ADDITIONThe solution was poured into ice
  2. 2
    抽出extracted with ethyl acetate (3×100 mL)
  3. 3
    洗浄The combined organic layer was washed with water, brine
  4. 4
    乾燥dried over sodium sulfate
  5. 5
    ろ過The solution was filtered
  6. 6
    その他evaporated the solvent
  7. 7
    その他The residue was chromatographed over silica gel column

実験手順

To an ice cold (0-5° C.) solution of ammonium hydroxide (35 mL) was added a solution of methyl 3-[(dimethylamino)diazenyl]-5-nitrothiophene-2-carboxylate (400 mg) in THF (10 mL) for 5 min and stirred at rt for 20 h. The solution was poured into ice cooled water and extracted with ethyl acetate (3×100 mL). The combined organic layer was washed with water, brine and dried over sodium sulfate. The solution was filtered and evaporated the solvent. The residue was chromatographed over silica gel column using hexane-ethyl acetate (50:50) as eluents to give the product as a yellow color solid (90 mg, 26%), mp 240-246° C. 1H NMR (400 MHz, DMSO-d6): δ 8.22 (1H, s), 8.05 (1H, s), 7.91 (1H, s), 3.63 (3H, s), 3.26 (3H, s); LC-MS (positive ion mode): m/z 266 (M+Na)+.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US08258119B2uspto-grants-2012_09