تفاعل #1509612

ord-b2f4b768c6bc4bb3a1ad6bc1f58b744b

معادلة التفاعل

CCOC(=O)CCC(C(=O)OCC)N1CCN(CC(=O)OCC)CCN(CC(=O)OCC)Cc2cccc(n2)C1
compound
CCOC(=O)CCC(C(=O)OCC)N1CCN(CC(=O)OCC)CCN(CC(=O)OCC)Cc2cccc(n2)C1
2-(6,9-Bisethoxycarbonylmethyl-3,6,9,15-tetraazabicyclo[9.3.1]pentadeca-1(15),11,13-trien-3-yl)pentanedioic acid diethyl ester
[Na+].[OH-]
sodium hydroxide
O=C(O)CCC(C(=O)O)N1CCN(CC(=O)O)CCN(CC(=O)O)Cc2cccc(n2)C1
2-(6,9-Biscarboxymethyl-3,6,9,15-tetraazabicyclo[9.3.1]pentadeca-1(15),11,13-trien-3-yl)pentanedioic acid
المردود 60.0%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةto reflux for 24 h
  2. 2
    workup.ADDITIONby adding weakly acidic resin
  3. 3
    ترشيحThe resin is filtered off
  4. 4
    غسيلwashed with water
  5. 5
    workup.ADDITIONA strongly basic resin is added to the filtrate
  6. 6
    ترشيحfiltered off
  7. 7
    غسيلwashed twice with water
  8. 8
    غسيلThe product is eluted with 50% acetic acid
  9. 9
    أخرىAfter evaporation to dryness
  10. 10
    أخرىthe product is obtained in the form of brown crystals

الإجراء التجريبي

15 mg of the compound obtained in stage 2 (26.5 μmol) are dissolved in 40 μl of ethanol and 53 μl of 5N sodium hydroxide are added dropwise rapidly. The mixture is brought to reflux for 24 h. The reaction medium is diluted 10-fold with water and the pH is then adjusted to 6.5 by adding weakly acidic resin. The resin is filtered off and washed with water. A strongly basic resin is added to the filtrate and then filtered off and washed twice with water. The product is eluted with 50% acetic acid. After evaporation to dryness, the product is obtained in the form of brown crystals. m=8 mg. Yield=60%.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08926945B2uspto-grants-2015_01