تفاعل #8629

ord-dd4587f83f314674afb5cfab26dbd8f9

معادلة التفاعل

CCN=C=NCCCN(C)C
1-(3-dimethylaminopropyl)-3-ethylcarbodiimide
CNC(=O)C(Cc1ccc2ccccc2c1)N1CCN(C(=O)C(N)Cc2ccc(F)cc2)C(CCOC(C)=O)C1
acetic acid 2-{1-[2-amino-3-(4-fluorophenyl)propionyl]-4-(1-methylcarbamoyl-2-naphthalen-2-ylethyl)piperazin-2-yl}-ethyl ester
Oc1cccc2[nH]nnc12
hydroxybenzotriazole
CN1CCOCC1
N-methylmorpholine
O
water
CNC(=O)C(Cc1ccc2ccccc2c1)N1CCN(C(=O)C(Cc2ccc(F)cc2)NC(=O)C(Cc2ccccc2O)NC(C)=O)C(CCOC(C)=O)C1
acetic acid 2-[1-{2-[2-acetylamino-3-(hydroxyphenyl)propionyl-amino]-3-(4-fluorophenyl)propionyl}-4-(1-methylcarbamoyl-2-naphthalen-2-ylethyl)-piperazin-2-yl]ethyl ester

المذيبات

ظروف التفاعل

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

المعالجة

  1. 1
    درجة الحرارةto warm
  2. 2
    workup.STIRRINGstir at room temperature another 2 hours
  3. 3
    ترشيحthe resulting solid is collected by filtration
  4. 4
    workup.DISSOLUTIONre-dissolved in EtOAc
  5. 5
    استخلاصextracted with water
  6. 6
    أخرىdried
  7. 7
    تركيزconcentrated in vacuo
  8. 8
    أخرىto afford a residue which
  9. 9
    أخرىpurified over silica gel

الإجراء التجريبي

A solution of acetic acid 2-{1-[2-amino-3-(4-fluorophenyl)propionyl]-4-(1-methylcarbamoyl-2-naphthalen-2-ylethyl)piperazin-2-yl}-ethyl ester, 64, (54.9 g, 100 mmol), hydroxybenzotriazole (16.2 g, 120 mmol), and N-methylmorpholine (132 mL, 120 mmol) in DMF (150 mL) is cooled to 0° C. and 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide (24.9 g, 130 mmol) is slowly added. The resulting mixture is stirred for 2 hours at 0° C. then allowed to warm and stir at room temperature another 2 hours. The reaction solution is diluted with water and the resulting solid is collected by filtration, re-dissolved in EtOAc and extracted with water, dried and concentrated in vacuo to afford a residue which purified over silica gel.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07087759B2uspto-grants-2006_08