تفاعل #725877

ord-2d1bc0ac75dd440e8f3a6fd78cb87d38

معادلة التفاعل

Cc1ccccc1S(=O)(=O)n1cccc1C(=O)c1cc(NC(=O)C(F)(F)F)cc(NC(=O)C(F)(F)F)c1
N-toluenesulfonyl-2-(3,5-di(trifluoroacetylamino)benzoyl)pyrrole
[K+].[OH-]
KOH
Nc1cc(N)cc(C(=O)c2ccc[nH]2)c1
2-(3,5-diaminobenzoyl)pyrrole
المردود 65.0%

الكواشف

لا شيء

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةthe mixture was heated
  2. 2
    درجة الحرارةat reflux until TLC analysis
  3. 3
    أخرىThe crude product was purified by column chromatography (SiO2, CH2Cl2:MeOH)

الإجراء التجريبي

To a stirred EtOH (10 mL) solution of N-toluenesulfonyl-2-(3,5-di(trifluoroacetylamino)benzoyl)pyrrole (1.00 g, 1.83 mmol), was added 40% KOH solution (2 mL) and the mixture was heated at reflux until TLC analysis showed complete conversion. The resulting solution was cooled to room temperature and worked up as in Example 7. The crude product was purified by column chromatography (SiO2, CH2Cl2:MeOH) to afford the purified product 2-(3,5-diaminobenzoyl)pyrrole (237 mg, 65% yield). 1H NMR (500 MHz, CD3OD, 25° C.) δ 2.43 (s, 3H), 6.45 (m, 1H), 6.90 (m, 1H), 7.41 (d, 2H), 7.88 (m, 3H), 7.93 (d, 2H), 8.39 (t, 1H); 13C NMR (100 MHz, CD3OD, 25° C.) δ 104.8, 105.7, 109.4, 119.5, 125.2, 130.5, 139.8, 147.8, 186.0; HRMS (EI): m/z 201.0896 (100) {M}+.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07691292B2uspto-grants-2010_04