تفاعل #2313148

ord-2a4568408c574c2997bfee697ef91396

معادلة التفاعل

Cl.Cl.N=C(N)c1ccc(N)cc1
4-Aminobenzamidine di-HCl
CN(C)C=O
DMF
O=C1CCCC(=O)O1
glutaric anhydride
NN=Cc1ccc(NC(C=O)CCC(=O)O)cc1
product
المردود 50.0%
NN=Cc1ccc(NC(C=O)CCC(=O)O)cc1
4-[[4-(aminoiminomethyl)phenyl]-amino]-5-oxopentanoic acid
المردود 50.0%

المذيبات

ظروف التفاعل

درجة الحرارة
100°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.ADDITIONwere added
  2. 2
    أخرىto precipitate
  3. 3
    درجة الحرارةHeating
  4. 4
    workup.ADDITIONwater (25 mL) was added
  5. 5
    درجة الحرارةafter cooling to room temperature
  6. 6
    ترشيحAn abundant precipitate was filtered
  7. 7
    أخرىdried in a desiccator

الإجراء التجريبي

4-Aminobenzamidine di-HCl (1 g, 4.8 mmol) was added to dry DMF (20 mL). To this solution dry pyridine (5 mL) and glutaric anhydride (0.68 g, 5.3 mmol) followed by 10 mg dimethylaminopyridine (DMAP) were added. The product started to precipitate after heating for 1/2 h at 100° C. Heating was continued for 2 hr and water (25 mL) was added after cooling to room temperature. An abundant precipitate was filtered and dried in a desiccator to give 0.8 g, 50% of product as a white solid: H NMR (d6 -DMSO) δ 1.95 (m, 2H), 2.4 (m, 2H), 2.5 (m, 2H), 7.85 (s, 4H), 9.05 (bs, 2H), 9.25 (bs, 2H), 10.4 (s, 1H), MS(FAB) m/z 250.1 (MH+).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05344957uspto-grants-1994_09