تفاعل #805899

ord-049fff498c564f37b6548b05bb0d0ab3

معادلة التفاعل

Nc1cccc(C(=O)O)c1C(=O)O
3-aminophthalic acid
NC1CCCNC1=O
3-aminopiperidine-2-one
Nc1cccc2c1C(=O)N(C1CCCNC1=O)C2=O
desired product 28
المردود 35.0%
Nc1cccc2c1C(=O)N(C1CCCNC1=O)C2=O
4-amino-2-(2-oxopiperidin-3-yl)isoindoline-1,3-dione
المردود 35.0%

الكواشف

لا شيء

المذيبات

ظروف التفاعل

درجة الحرارة
90°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىVolatiles were removed in vacuo
  2. 2
    أخرىthe dark-brown crude residue was purified by preparative reverse phase HPLC

الإجراء التجريبي

To a solution of 3-aminophthalic acid (0.100 g, 0.552 mmol) in DMF (1.1 mL) was added 3-aminopiperidine-2-one (0.063 g, 0.552 mmol) and the reaction was stirred at 90° C. over 18 h. Volatiles were removed in vacuo and the dark-brown crude residue was purified by preparative reverse phase HPLC to give the desired product 28 (0.050 g, 35%) as an off-white powder. 1H NMR (400 MHz, DMSO) δ 7.83 (s, 1H), 7.43 (dd, J=8.3, 7.1 Hz, 1H), 7.07-6.87 (m, 2H), 6.47 (br s, 2H), 4.49 (dd, J=11.9, 6.3 Hz, 1H), 3.27-3.10 (m, 2H), 2.19 (dt, J=12.0, 7.7 Hz, 1H), 2.05-1.72 (m, 3H). MS (ESI) m/z calcd for C13H14N3O3 [M+H]+ 260.3, found: 260.9.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US09193989B2uspto-grants-2015_11