反応 #2467987

ord-8a333b08c5f24f25b312900400960658

反応方程式

O
water
[NH4+].[OH-]
ammonium hydroxide
COC(=O)c1cscc1N=NN(C)C
methyl 4-[(dimethylamino)diazenyl]thiophene-3-carboxylate
CN(C)N=Nc1cscc1C(N)=O
solid
収率 25.0%
CN(C)N=Nc1cscc1C(N)=O
4-[(Dimethylamino)diazenyl]thiophene-3-carboxamide
収率 25.0%

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 chloroform
  3. 3
    洗浄The combined chloroform 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 (5 mL) was added a solution of methyl 4-[(dimethylamino)diazenyl]thiophene-3-carboxylate (110 mg) in THF (2 mL) for 5 min and stirred at rt for 36 h. The solution was poured into ice cooled water and extracted with chloroform. The combined chloroform 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 chloroform-methanol (98:2) as eluents to give the product as a pale red color solid (25 mg, 25%), mp 168-172° C. IR (neat) νmax 3324, 3125, 2917, 2851, 1655, 1600, 1367, 1336, 1090 cm−1; 1H NMR (400 MHz, CDCl3): δ 8.55 (1H, br s), 8.19 (1H, d, J=3.6 Hz), 7.15 (1H, d, J=3.6 Hz), 5.84 (1H, br s), 3.56 (3H, br s), 3.19 (3H, br s); LC-MS (positive ion mode): m/z 199 (M+H)+.

出典

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