تفاعل #1980556

ord-bbaf32fc950b41069e287c55bc85af13

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةwas heated
  2. 2
    درجة الحرارةat reflux for 3 h
  3. 3
    أخرىThe solvent was evaporated
  4. 4
    أخرىthe residue was triturated in tert-butyl methyl ether
  5. 5
    أخرىThe precipitate was removed by filtration
  6. 6
    تركيزthe filtrate was concentrated to dryness
  7. 7
    أخرىThe residue was crystallized from hot ethanol

الإجراء التجريبي

A mixture of 7-chloro-2-oxo-1,2,3,5-tetrahydro-benzo[1,4]diazepine-4-carboxylic acid tert-butyl ester (41.1 g, 0.139 mol) and 2,4-bis-(4-methoxyphenyl)-1,3,2,4-dithiadiphosphetane-2,4-disulfide (31.5 g, 0.0763 mol) in tetrahydrofuran (1100 ml) was heated at reflux for 3 h. The solvent was evaporated and the residue was triturated in tert-butyl methyl ether. The precipitate was removed by filtration and the filtrate was concentrated to dryness. The residue was crystallized from hot ethanol to give the title compound (37.5 g, 86.4%) as light yellow solid. MS m/e: 311 (M−H+).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08513238B2uspto-grants-2013_08