تفاعل #465959

ord-6ac3d530c09e4333b5f41c578e14f103

معادلة التفاعل

COC(=O)c1nc(Br)cc(N)c1Cl
methyl 4-amino-6-bromo-3-chloropyridine-2-carboxylate
[Na+].[OH-]
NaOH
Nc1cc(Br)nc(C(=O)O)c1Cl
4-amino-6-bromo-3-chloropyridine-2-carboxylic acid
المردود 34.8%

الكواشف

لا شيء

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىevaporated to dryness in vacuo
  2. 2
    workup.DISSOLUTIONThe residue was dissolved in water
  3. 3
    أخرىAfter separation of the phases
  4. 4
    أخرىThe aqueous layer was evaporated to dryness
  5. 5
    workup.DISSOLUTIONthe residue was dissolved in 50 mL of methanol
  6. 6
    ترشيحfiltered
  7. 7
    أخرىThe filtrate was evaporated under reduced pressure
  8. 8
    أخرىthe residue was triturated with 5 percent diethyl ether in petroleum ether

الإجراء التجريبي

To methyl 4-amino-6-bromo-3-chloropyridine-2-carboxylate (200mg; 0.8 mmol) in 10 mL of methanol was added excess 2N NaOH (10 mL). The mixture was stirred for 1 hr at ambient temperature and then evaporated to dryness in vacuo. The residue was dissolved in water and diethyl ether. After separation of the phases, the aqueous layer was acidified with 1N HCl to a pH=2. The aqueous layer was evaporated to dryness and the residue was dissolved in 50 mL of methanol and filtered. The filtrate was evaporated under reduced pressure and the residue was triturated with 5 percent diethyl ether in petroleum ether to give 70 mg of 4-amino-6-bromo-3-chloropyridine-2-carboxylic acid, mp 182-183° C.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US06297197B1uspto-grants-2001_10