2-(6-Hydroxy-3-oxo-3H-xanthen-9-yl)benzoic acid → 5-Fam

HRID 62482

반응식

HRID 62482 반응식
N[C@H]([C:8]([OH:10])=[O:9])CCCCN.NN.[CH:13]1[C:18](N=C=S)=[CH:17][C:16]2[C:22]([O:24][C:25]3([C:35]4[CH:36]=[CH:37][C:38]([OH:40])=[CH:39][C:34]=4[O:33][C:27]4[CH:28]=[C:29]([OH:32])[CH:30]=[CH:31][C:26]3=4)[C:15]=2[CH:14]=1)=[O:23].C(N(C(C)C)CC)(C)C.C1C=CC(C(O)=O)=C(C2C3C=CC(O)=CC=3OC3C=2C=CC(C=3)=O)C=1>CN(C=O)C>[CH:13]1[C:18]([C:8]([OH:10])=[O:9])=[CH:17][C:16]2[C:22]([O:24][C:25]3([C:35]4[CH:36]=[CH:37][C:38]([OH:40])=[CH:39][C:34]=4[O:33][C:27]4[CH:28]=[C:29]([OH:32])[CH:30]=[CH:31][C:26]3=4)[C:15]=2[CH:14]=1)=[O:23]

참가 물질

7

실험 절차

Peptide-resin obtained via Method 5, containing an ivDde protecting group on the epsilon nitrogen of lysine, was mixed with a solution of hydrazine in DMF (10% hydrazine/DMF, 2×10 mL, 10 min) to remove the ivDde group. The epsilon nitrogen of the lysine was labeled with fluorescein-5-isothiocyanate (0.12 mmol) and diisopropylethylamine (0.12 mmol) in DMF. The mixture was agitated for 12 h (fluorescein-containing compounds were protected from light). The resin was then washed with DMF (3×10 mL) and twice with CH2Cl2 (10 mL) and dried under nitrogen for 1 h. The peptide was cleaved from the resin using reagent B for 4 h and the solution collected by filtration. The volatiles were removed under reduced pressure, and the residue was dried under vacuum. The peptide was precipitated with ether, collected and the precipitate was dried under a stream of nitrogen. The precipitate was added to water (1 mg/mL) and the pH of the mixture was adjusted to 8 with 10% aqueous meglumine. Cyclization of the peptide was carried out for 48 h and the solution was freeze-dried. The crude cyclic peptide was dissolved in water and purified by RP-HPLC on a C18 column with a linear gradient of acetonitrile into water (both phases contained 0.1% TFA). Fractions containing the pure product were collected and freeze-dried. The peptides were characterized by ES-MS and the purity was determined by RP-HPLC (linear gradient of acetonitrile into water/0.1% TFA).

후처리

  1. customto remove the ivDde group
  2. washThe resin was then washed with DMF (3×10 mL) and twice with CH2Cl2 (10 mL)
  3. customdried under nitrogen for 1 h
  4. customfor 4 h
  5. filtrationthe solution collected by filtration
  6. customThe volatiles were removed under reduced pressure
  7. customthe residue was dried under vacuum
  8. customThe peptide was precipitated with ether
  9. customcollected
  10. customthe precipitate was dried under a stream of nitrogen
  11. additionThe precipitate was added to water (1 mg/mL)
  12. waitCyclization of the peptide was carried out for 48 h
  13. customthe solution was freeze-dried
  14. dissolutionThe crude cyclic peptide was dissolved in water
  15. custompurified by RP-HPLC on a C18 column with a linear gradient of acetonitrile into water (both phases
  16. additionFractions containing the pure product
  17. customwere collected
  18. customfreeze-dried

출처 및 근거

ORD 기록
ord-857ac6af9c87414abc6de0fec7d0c4a1
출처 데이터셋
uspto-grants-2016_09
특허 번호
US09446155B2

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