تفاعل #40278

ord-be1165b7684041fa91ec2ef11dffc25a

معادلة التفاعل

CC(C)(C)C(=O)Nc1cnc(C(=O)CBr)cn1
compound
CC(C)(C)C(=O)Nc1cnc(C(=O)CBr)cn1
N-[5-(2-bromo-acetyl)-pyrazin-2-yl]-2,2-dimethyl-propionamide
CC(=O)O
acetic acid
CN(C)C=O
DMF
CC(=O)[O-].[Na+]
sodium acetate
CC(=O)OCC(=O)c1cnc(NC(=O)C(C)(C)C)cn1
title compound
المردود 90.9%
CC(=O)OCC(=O)c1cnc(NC(=O)C(C)(C)C)cn1
acetic acid 2-[5-(2,2-dimethylpropionylamino)-pyrazin-2-yl]-2-oxo-ethyl ester
المردود 90.9%

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىA 500 mL round bottomed flask equipped with a magnetic stirrer, addition funnel
  2. 2
    أخرىreaction
  3. 3
    workup.ADDITIONwas added
  4. 4
    workup.STIRRINGwith stirring
  5. 5
    أخرىThe organic layer was separated
  6. 6
    غسيلwashed with 3×100 mL of water
  7. 7
    تركيزconcentrated at 30° C./60 mmHg to a volume of ca. 60 mL
  8. 8
    workup.ADDITIONThe resulting slurry was diluted with 200 mL of heptane
  9. 9
    تركيزconcentrated at 30° C./60 mmHg to a volume of ca. 150 mL
  10. 10
    workup.STIRRINGstirred at 50° C. for 30 min
  11. 11
    درجة الحرارةAfter cooling to room temperature
  12. 12
    ترشيحthe solid was collected by filtration
  13. 13
    غسيلwashed with 40 mL of 10% ethyl acetate in heptane
  14. 14
    أخرىdried by suction
  15. 15
    workup.WAITunder reduced pressure (house vacuum) for 24 h

الإجراء التجريبي

A 500 mL round bottomed flask equipped with a magnetic stirrer, addition funnel, thermocouple probe and nitrogen inlet/outlet was charged with 4.40 mL (76.86 mmol) of acetic acid, 140 mL of DMF and 7.000 g (85.33 mmol) of sodium acetate. Then, 23.30 g (77.62 mmol) of the compound obtained in step 5 was added portionwise over 45 min. After stirring at room temperature for an additional 1 h, HPLC analysis indicated complete reaction. The reaction mixture was diluted with 350 mL of ethyl acetate and 100 mL of saturated sodium bicarbonate was added with stirring. The organic layer was separated, washed with 3×100 mL of water and concentrated at 30° C./60 mmHg to a volume of ca. 60 mL. The resulting slurry was diluted with 200 mL of heptane, concentrated at 30° C./60 mmHg to a volume of ca. 150 mL, and stirred at 50° C. for 30 min. After cooling to room temperature, the solid was collected by filtration, washed with 40 mL of 10% ethyl acetate in heptane and dried by suction, then under reduced pressure (house vacuum) for 24 h, to give 19.52 g (90.0% yield) of the title compound as an off-white solid; 98.81% pure as determined by HPLC analysis (same conditions as in step 4, retention time 6.78 min).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07727750B2uspto-grants-2010_06