تفاعل #55421

ord-f11b8c37a12540549fe51ebc977465c0

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.ADDITIONTo a suspension of 19.3 g
  2. 2
    أخرىThe precipitate is removed by filtration
  3. 3
    أخرىthe filtrate is evaporated
  4. 4
    أخرىto give a residue which
  5. 5
    ترشيحof benzene and filtered again
  6. 6
    استخلاصThe filtrate is extracted with three 100 ml
  7. 7
    workup.ADDITIONthe pH is adjusted to 7.5 by addition of solid sodium bicarbonate
  8. 8
    أخرىThe organic layer is separated
  9. 9
    استخلاصthe aqueous phase is extracted with two 150 ml
  10. 10
    تجفيفThe combined extracts are dried (MgSO4)
  11. 11
    ترشيحfiltered
  12. 12
    أخرىevaporated to dryness

الإجراء التجريبي

To a suspension of 19.3 g. (0.05 mol.) of 7-amino-3-[1-(2-carbamoylethyl)tetrazol-5-ylthiomethyl]-3-cephem-4-carboxylic acid in 500 ml. of dry methylene chloride is added in one portion 30.0 g. (0.15 mol.) of O-t-butyldiisopropylpseudourea in 50 ml. of methylene chloride and the mixture is stirred at ambient temperature for 24 hours. The precipitate is removed by filtration and the filtrate is evaporated to give a residue which is taken up in 200 ml. of benzene and filtered again. The filtrate is extracted with three 100 ml. portions of cold 1N hydrochloric acid. The aqueous extracts are layered with ethyl acetate and the pH is adjusted to 7.5 by addition of solid sodium bicarbonate. The organic layer is separated and the aqueous phase is extracted with two 150 ml. portions of ethyl acetate. The combined extracts are dried (MgSO4), filtered and evaporated to dryness to give 7-amino-3-[1-(2-carbamoylethyl)tetrazol-5-ylthiomethyl]-3-cephem-4-carboxylic acid t-butyl ester.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US04220644uspto-grants-1980_09