Реакция #2467987

ord-8a333b08c5f24f25b312900400960658

Уравнение реакции

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
Выход 25.0%
CN(C)N=Nc1cscc1C(N)=O
4-[(Dimethylamino)diazenyl]thiophene-3-carboxamide
Выход 25.0%

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    workup.ADDITIONThe solution was poured into ice
  2. 2
    Экстракцияextracted with chloroform
  3. 3
    ПромывкаThe combined chloroform layer was washed with water, brine
  4. 4
    Сушкаdried over sodium sulfate
  5. 5
    ФильтрацияThe solution was filtered
  6. 6
    Другоеevaporated the solvent
  7. 7
    ДругоеThe residue was chromatographed over silica gel column

Методика

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)+.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US08258119B2uspto-grants-2012_09