تفاعل #1098

ord-a05cf5e0c43f4ae0a2ddb5d7e074dffb

معادلة التفاعل

COc1c(NOCc2ccccc2)ccnc1C
4-(O-benzylhydroxylamino)-3-methoxy-2-methylpyridine
[H-].[Na+]
sodium hydride
Cc1ccc(S(=O)(=O)OC2CCC3(CC2)OCC(C)(C)CO3)cc1
3,3-dimethyl-9-tosyloxy-1,5-dioxaspiro[5.5]undecane
[H][H]
hydrogen
COc1c(N(OCc2ccccc2)C2CCC3(CC2)OCC(C)(C)CO3)ccnc1C
4-[O-Benzyl-N-(3,3-dimethyl-1,5-dioxaspiro[5.5]undec-9-yl)hydroxylamino]-3-methoxy-2-methylpyridine

المذيبات

ظروف التفاعل

درجة الحرارة
50°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.DISTILLATIONThe THF is then distilled off in vacuo
  2. 2
    workup.ADDITIONthe mixture is poured into water
  3. 3
    استخلاصAfter extracting with methylene chloride
  4. 4
    أخرىthe product is purified by chromatography on silica gel (ethyl acetate)

الإجراء التجريبي

7.3 g of 4-(O-benzylhydroxylamino)-3-methoxy-2-methylpyridine in 30 ml of absolute DMSO are deprotonated under N2 using 0.9 g of sodium hydride (80% strength). After evolution of hydrogen has ended, 11.7 g of 3,3-dimethyl-9-tosyloxy-1,5-dioxaspiro[5.5]undecane are added in 50 ml of absolute THF. The mixture is stirred at room temperature for 1 hour and at 50° C. for 4 hours. The THF is then distilled off in vacuo and the mixture is poured into water. After extracting with methylene chloride, the product is purified by chromatography on silica gel (ethyl acetate). 6.5 g=51%

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05723450uspto-grants-1998_03