反応 #40278

ord-be1165b7684041fa91ec2ef11dffc25a

反応方程式

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
収率 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
収率 90.9%

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他A 500 mL round bottomed flask equipped with a magnetic stirrer, addition funnel
  2. 2
    その他reaction
  3. 3
    workup.ADDITIONwas added
  4. 4
    workup.STIRRINGwith stirring
  5. 5
    その他The organic layer was separated
  6. 6
    洗浄washed with 3×100 mL of water
  7. 7
    濃縮concentrated 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
    濃縮concentrated at 30° C./60 mmHg to a volume of ca. 150 mL
  10. 10
    workup.STIRRINGstirred at 50° C. for 30 min
  11. 11
    温度After cooling to room temperature
  12. 12
    ろ過the solid was collected by filtration
  13. 13
    洗浄washed with 40 mL of 10% ethyl acetate in heptane
  14. 14
    その他dried by suction
  15. 15
    workup.WAITunder reduced pressure (house vacuum) for 24 h

実験手順

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).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US07727750B2uspto-grants-2010_06