تفاعل #2045118

ord-94dd8f0baa6944cc87a7d2e95a69141f

معادلة التفاعل

Cc1cc([N+](=O)[O-])ccc1F
4-fluoro-3-methylnitrobenzene
CN1CCNCC1
N-methylpiperazine
[Cl-].[Na+]
NaCl
Cc1cc([N+](=O)[O-])ccc1N1CCN(C)CC1
4-(4-methylpiperazinyl)-3-methylnitrobenzene
المردود 92.3%

الكواشف

لا شيء

المذيبات

ظروف التفاعل

درجة الحرارة
120°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةThe reaction mixture upon cooling to room temperature
  2. 2
    أخرىThe resulting solid was sonicated for approx. 30 seconds
  3. 3
    ترشيحfiltered
  4. 4
    غسيلwashed with ice-cold water (2×10 mL)
  5. 5
    أخرىdried under high vacuum

الإجراء التجريبي

A homogeneous mixture of 4-fluoro-3-methylnitrobenzene 1 (20 g, 129 mmol) and N-methylpiperazine 3 (25.82 g, 258 mmol) in N-methylpyrrolidone (NMP) (10 mL) was refluxed (120° C.) under N2 for 24 hours. The reaction mixture upon cooling to room temperature was poured over a saturated NaCl solution (100 mL). The resulting solid was sonicated for approx. 30 seconds, filtered, washed with ice-cold water (2×10 mL) and dried under high vacuum to obtain 4-(4-methylpiperazinyl)-3-methylnitrobenzene 5 (28 g, 92%). 1H NMR (CD3OD): δ 8.02 (m, 2H), 7.13 (d, 1H, J=9.3 Hz), 3.08 (m, 4H), 2.66 (m, 4H), 2.38 (s, 6H); LCMS: purity: 99%, MS (m/e): 236 (MH+).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08410093B2uspto-grants-2013_04