반응 #2467987

ord-8a333b08c5f24f25b312900400960658

반응 방정식

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

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.ADDITIONThe solution was poured into ice
  2. 2
    추출extracted with chloroform
  3. 3
    세척The combined chloroform layer was washed with water, brine
  4. 4
    건조dried over sodium sulfate
  5. 5
    여과The solution was filtered
  6. 6
    기타evaporated the solvent
  7. 7
    기타The residue was chromatographed over silica gel column

실험 절차

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)+.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08258119B2uspto-grants-2012_09