تفاعل #4312

ord-fefe59a7cdf245f1bf02e5ac9fe770f6

معادلة التفاعل

NCCS(=O)(=O)c1ccccc1
2-(phenylsulfonyl)ethanamine
O=C(n1ccnc1)n1ccnc1
1,1'-carbonyldiimidazole
O=C(O)CC(O)(CC(=O)O)C(=O)O
citric acid
CCNCCN(CC)CC
N,N,N'-triethylethylenediamine
CCN(CC)CCN(CC)C(=O)NCCS(=O)(=O)c1ccccc1.O=C(O)CC(O)(CC(=O)O)C(=O)O
white crystalline solid
المردود 52.0%
CCN(CC)CCN(CC)C(=O)NCCS(=O)(=O)c1ccccc1.O=C(O)CC(O)(CC(=O)O)C(=O)O
N-[2-(Diethylamino)ethyl]-N-ethyl-N'-[2-(phenylsulfonyl)ethyl]urea citrate
المردود 52.0%

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةthe mixture was refluxed for 16 hr
  2. 2
    أخرىThe solvent was removed in vacuo
  3. 3
    أخرىthe residue was partitioned between a mixture of 300 ml of methylene chloride and 500 ml of ether and water
  4. 4
    تجفيفThe organic phase was dried over magnesium sulfate
  5. 5
    أخرىthe solvent was removed in vacuo
  6. 6
    أخرىto give an oil
  7. 7
    workup.ADDITIONwas added
  8. 8
    أخرىA white precipitate formed

الإجراء التجريبي

A solution of 5.55 g (0.030 mole) of 2-(phenylsulfonyl)ethanamine and 5.35 g (0.033 mole) of 1,1'-carbonyldiimidazole in 400 ml of tetrahydrofuran was stirred at room temperature for 1 hr. A solution of 4.62 g (0.032 mole) of N,N,N'-triethylethylenediamine in 50 ml of tetrahydrofuran was added, and the mixture was refluxed for 16 hr. The solvent was removed in vacuo, and the residue was partitioned between a mixture of 300 ml of methylene chloride and 500 ml of ether and water. The organic phase was dried over magnesium sulfate, and the solvent was removed in vacuo to give an oil. A solution of the oil in methanol was treated with an equivalent of citric acid and ether was added. A white precipitate formed to give 8.54 g (52.0%) of white crystalline solid, m.p. 105°-107° C.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US04724235uspto-grants-1988_02