تفاعل #1135847

ord-8497d7cfd23e4c10960dc9f2f68a1214

معادلة التفاعل

O=C([O-])O.[Na+]
NaHCO3
CC(=O)[O-].[Na+]
NaOAc
BrBr
bromine
Nc1ccncc1[N+](=O)[O-]
3-nitropyridin-4-amine
Nc1c(Br)cncc1[N+](=O)[O-]
3-bromo-5-nitropyridin-4-amine
المردود 77.0%

الكواشف

لا شيء

المذيبات

ظروف التفاعل

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

المعالجة

  1. 1
    workup.ADDITIONwas added to a sealed tube
  2. 2
    أخرىconsumption of starting material
  3. 3
    تركيزThe reaction mixture was concentrated
  4. 4
    أخرىto obtain a solid which
  5. 5
    استخلاصextracted with ethyl acetate
  6. 6
    أخرىThe combined organic extracts were dried
  7. 7
    تركيزconcentrated

الإجراء التجريبي

A mixture of 3-nitropyridin-4-amine (XII) (10 g, 71.94 mmol) and acetic acid (120 ml) was added to a sealed tube followed by addition of NaOAc (29.50 g, 93.52 mmol) and dropwise addition of bromine (4.7 ml 359.7 mmol) under stirring. The sealed tube was heated at 100° C. for 28 h until TLC showed consumption of starting material. The reaction mixture was concentrated to obtain a solid which was dissolved in water, basified with NaHCO3 and extracted with ethyl acetate. The combined organic extracts were dried and concentrated to produce 3-bromo-5-nitropyridin-4-amine (XIII) as a yellow solid (12 g, 55 mmol, 77% yield). 1H NMR (DMSO-d6) δ ppm 9.19 (s, 1H), 8.58 (s, 1H); ESIMS found for C5H4BrN3O2 m/z 217, 219 (M+, M+2).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US09381192B2uspto-grants-2016_07