반응 #1552039

ord-c861b1f4a1a444aeb63ce16e0284ec69

반응 방정식

O=C(O)C(F)(F)F
trifluoroacetic acid
CCCCCCCCCCCCCCCC(=O)ONCC(=O)OC1CC(=O)NC1=O
N-palmitoyloxy-glycyloxysuccinimide
N[C@@H](Cc1c[nH]cn1)C(=O)O
L-histidine
CCN(CC)CC
triethylamine
CCCCCCCCCCCCCCCC(=O)NCC(=O)N[C@@H](Cc1c[nH]cn1)C(=O)O.O=C(O)C(F)(F)F
colorless solid
수율 54.0%
CCCCCCCCCCCCCCCC(=O)NCC(=O)N[C@@H](Cc1c[nH]cn1)C(=O)O.O=C(O)C(F)(F)F
N-palmitoyl-Gly-His TFA
수율 54.0%

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도while cooled with ice
  2. 2
    workup.ADDITIONwas added
  3. 3
    온도while cooled with ice
  4. 4
    workup.STIRRINGby stirring for another 17 hours
  5. 5
    여과The precipitated solid was filtered off as it
  6. 6
    기타to obtain a solid
  7. 7
    workup.STIRRINGby stirring
  8. 8
    세척to be washed with 2 L of water three times
  9. 9
    기타was subsequently dried under reduced pressure
  10. 10
    기타The resulting dry solid
  11. 11
    workup.DISSOLUTIONwas dissolved in 400 mL of trifluoroacetic acid
  12. 12
    여과a small amount of insoluble matter was filtered off with a membrane
  13. 13
    여과filter
  14. 14
    농축The filtrate was concentrated under reduced pressure to about half the amount, which
  15. 15
    세척was then washed with diethyl ether
  16. 16
    기타The solid was dried under reduced pressure
  17. 17
    세척was washed with water an appropriate number of times
  18. 18
    기타the resulting solid was dried under reduced pressure

실험 절차

198 g of the N-palmitoyloxy-glycyloxysuccinimide synthesized above as a whole was suspended in DMF and, to the resultant solution while cooled with ice with stirring, a suspension of 113 g (0.728 mol) of L-histidine, 55.6 mL (0.400 mol) of triethylamine, and 350 ml of water was added. Subsequently, the resultant solution was stirred for 30 minutes while cooled with ice, and the temperature was then raised to room temperature, followed by stirring for another 17 hours. The precipitated solid was filtered off as it was to obtain a solid. The resultant product was added to a mixed solution of 120 mL of trifluoroacetic acid and 1.5 L of ice water, followed by stirring and then filtering insoluble matter. The resulting solid was placed in a jug to be washed with 2 L of water three times, and was subsequently dried under reduced pressure. The resulting dry solid was dissolved in 400 mL of trifluoroacetic acid, and a small amount of insoluble matter was filtered off with a membrane filter. The filtrate was concentrated under reduced pressure to about half the amount, which was then washed with diethyl ether. The solid was dried under reduced pressure and was washed with water an appropriate number of times, and the resulting solid was dried under reduced pressure to obtain 112 g (54%) of a colorless solid.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08999300B2uspto-grants-2015_04