تفاعل #2467992

ord-03c51e4e4cf3494793c65fa351d44ece

معادلة التفاعل

[Cl-].[NH4+]
ammonium chloride
Cn1nnc2sc([N+](=O)[O-])cc2c1=O
3-methyl-6-nitrothiopheno[2,3-d]1,2,3-triazin-4-one
Cl
Hydrochloric acid
Cn1nnc2sc(N)cc2c1=O
solid
المردود 7.5%
Cn1nnc2sc(N)cc2c1=O
6-amino-3-methylthiopheno[2,3-d]1,2,3-triazin-4-one
المردود 7.5%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةwarmed to 70 for 1 h
  2. 2
    ترشيحThe solution was filtered
  3. 3
    استخلاصThe solution was extracted with ethyl acetate (4×100 mL)
  4. 4
    تجفيفThe combined organic layer was dried over sodium sulfate
  5. 5
    ترشيحfiltered
  6. 6
    أخرىSolvent was evaporated
  7. 7
    أخرىthe residue was chromatographed over silica gel column

الإجراء التجريبي

To a solution of 3-methyl-6-nitrothiopheno[2,3-d]1,2,3-triazin-4-one (1.25 g, 5.9 mmol) in methanol (50 mL) was added conc. Hydrochloric acid (0.6 mL). To the above solution was added iron powder (1.67 g, 29.5 mmol) followed by a solution of ammonium chloride (1.57 g, 29.5 mmol) in water (10 mL) at rt. The reaction mixture was stirred and warmed to 70 for 1 h and was then allowed to cool to rt. The solution was filtered and basified with saturated sodium bicarbonate solution. The solution was extracted with ethyl acetate (4×100 mL). The combined organic layer was dried over sodium sulfate and filtered. Solvent was evaporated and the residue was chromatographed over silica gel column using hexane-ethyl: acetate (60:40) as eluents to give the product as a pale yellow color solid (80 mg, 7.5%), mp 190-194° C. 1H NMR (400 MHz, DMSO-d6): δ 7.40 (2H, s), 6.11 (1H, s), 3.82 (3H, s); LC-MS (negative ion mode): m/z 181 (M−H)−.

المصدر

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