Piperidine → L-Glutamic Acid

HRID 1886842Notes

Reaction equation

HRID 1886842 reaction equation
N1CCCC[CH2:2]1.CN(C(ON1N=NC2C=CC=NC1=2)=[N+](C)C)C.F[P-](F)(F)(F)(F)F.C(N(CC)C(C)C)(C)C.[OH:40][C:41]([C:43](F)(F)F)=[O:42].[N:47]1([CH2:53][C:54]([OH:56])=[O:55])CCNCC1>CN(C=O)C.CN1C(=O)CCC1>[NH2:47][C@H:53]([C:54]([OH:56])=[O:55])[CH2:2][CH2:43][C:41](=[O:42])[OH:40]

Participants

7

Procedure

Approximately 10 mg of Fmoc-Glu-Fib-Trityl-chloride resin was treated with 20% (v/v) piperidine in DMF (2 mL×1 min, filtered, then 2 mL×5 min), filtered and washed (NMP). Fmoc-cysteic-acid (10 eqv to Glu-Fib amount on the resin) was individually activated with HATU (P/N: Applied Biosystems 4317033, 9.5 eqv) and N, N-Diisopropylethylamine (30 eqv) in NMP (˜1 mL), added to the resin and mixed for 30 min. Resin was then filtered, washed with NMP, and Fmoc group was cleaved. Piperazine acetic acid-TFA salt (10 eqv) was then activated using HATU (9.5 eqv) and N,N-Diisopropylethylamine (60 eqv) in NMP (˜1.5 mL), and added to the resin. After 30 min the resin was washed with NMP followed by CH3CN. Conjugated peptide was cleaved (and deprotected) from resin using 95:5 TFA-water (200 μL, 2 h) and precipitated using Et2O. Analysis of compound (47) was performed using ES-MS (direct infusion in water, Calculated [M+H]+=2070.9, Observed [M+H]+=2071.8)

Workup

  1. filtrationfiltered
  2. filtration2 mL×5 min), filtered
  3. washwashed (NMP)
  4. additionadded to the resin
  5. additionmixed for 30 min
  6. filtrationResin was then filtered
  7. washwashed with NMP, and Fmoc group
  8. additionadded to the resin
  9. washAfter 30 min the resin was washed with NMP
  10. custom95:5 TFA-water (200 μL, 2 h)
  11. customprecipitated

Sources & evidence

ORD record
ord-0353a5ae653c4feaa6806e740ed2f94e
Source dataset
uspto-grants-2013_08
Patent number
US08501498B2

Reaction notes

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