تفاعل #1478575

ord-759f972a92ab4b6e88f73095ee87a70f

معادلة التفاعل

O=[N+]([O-])c1ccc(F)cc1
4-fluoronitrobenzene
CN1CCCC1
N-methyl-pyrrolidine
CN1CCN(CCCN)CC1
N-(3-aminopropyl)-N′-methylpiperazine
O=C([O-])[O-].[K+].[K+]
K2CO3
CN1CCN(CCCNc2ccc([N+](=O)[O-])cc2)CC1
N-[3-(4-methyl-piperazin-1-yl)propyl]-4-nitro-1-aminobenzene
المردود 81.6%
CN1CCN(CCCNc2ccc([N+](=O)[O-])cc2)CC1
N-[3-(4-methylpiperazin-1-yl)propyl]-4-nitro-1-aminobenzene
المردود 81.6%

المذيبات

ظروف التفاعل

درجة الحرارة
60°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةafter cooling to room temperature
  2. 2
    أخرىThe yellow precipitate formed
  3. 3
    ترشيحwas filtered off
  4. 4
    تجفيفdried over P2O5

الإجراء التجريبي

2 g of 4-fluoronitrobenzene were added to a solution of 20 ml of N-methyl-pyrrolidine, 2.67 g of N-(3-aminopropyl)-N′-methylpiperazine and 2.35 g of K2CO3. The reaction medium was heated at 60° C. for 10 hours and, after cooling to room temperature, was then poured into a water and ice mixture. The yellow precipitate formed was filtered off, reslurried in water and then dried over P2O5. 3.22 g of N-[3-(4-methyl-piperazin-1-yl)propyl]-4-nitro-1-aminobenzene (9) were obtained.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07338536B2uspto-grants-2008_03