تفاعل #2467987

ord-8a333b08c5f24f25b312900400960658

معادلة التفاعل

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

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.ADDITIONThe solution was poured into ice
  2. 2
    استخلاصextracted with chloroform
  3. 3
    غسيلThe combined chloroform layer was washed with water, brine
  4. 4
    تجفيفdried over sodium sulfate
  5. 5
    ترشيحThe solution was filtered
  6. 6
    أخرىevaporated the solvent
  7. 7
    أخرىThe residue was chromatographed over silica gel column

الإجراء التجريبي

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)+.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08258119B2uspto-grants-2012_09