تفاعل #1543035

ord-86b6ededcd9143a68cc465ab143d5135

معادلة التفاعل

O
water
O=C(O)CN(CCN1CC(=O)OC(=O)C1)CCN1CC(=O)OC(=O)C1
1.5-bis(2,6-dioxomorpholino)-3-carboxymethyl-3-azapentane
CCN(CC)CC
triethylamine
CCOC(=O)CCCCCCCCCCN
11-aminoundecanoic acid ethyl ester
CCOC(=O)CCCCCCCCCCNC(=O)CN(CCN(CCN(CC(=O)O)CC(=O)O)CC(=O)O)CC(=O)O
title compound
CCOC(=O)CCCCCCCCCCNC(=O)CN(CCN(CCN(CC(=O)O)CC(=O)O)CC(=O)O)CC(=O)O
3,6-Bis(carboxymethyl)-9-(10-carbethoxydecylcarbamoylmethyl)-3,6,9-triazaundecanedioic acid

المذيبات

ظروف التفاعل

درجة الحرارة
0°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةThe solution is heated for 3 hours to 70° C.
  2. 2
    أخرىthe solution is evaporated to dryness in a vacuum
  3. 3
    workup.ADDITIONthe solution is mixed by drops with concentrated hydrochloric acid until permanent cloudiness
  4. 4
    workup.STIRRINGAfter stirring overnight in the ice bath
  5. 5
    غسيلwashed with water
  6. 6
    أخرىdried in a vacuum at 50° C

الإجراء التجريبي

17.85 g (50 mmol) of 1.5-bis(2,6-dioxomorpholino)-3-carboxymethyl-3-azapentane is stirred in 200 ml of dimethylformamide and mixed with 9 ml (50 mmol) of water. The solution is heated for 3 hours to 70° C., cooled off to 0° C. and 36.07 ml (260 mmol) of triethylamine and 10.8 g (50 mmol) of 11-aminoundecanoic acid ethyl ester are added. After stirring overnight at room temperature, the solution is evaporated to dryness in a vacuum. The residue is taken up in 100 ml of water and the solution is mixed by drops with concentrated hydrochloric acid until permanent cloudiness. After stirring overnight in the ice bath, the finely crystalline precipitate is suctioned off, washed with water and dried in a vacuum at 50° C. 14.9 g (65% of theory) of the title compound is obtained as a white powder with melting point 155°-157° C.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05843399uspto-grants-1998_12