Piperidine → L-Glutamic Acid
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
Reactant 4
Product 1
Reagents, catalysts & solvents 2
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). Compound (43f) (10 eqv to Glu-Fib amount on the resin) was 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 the 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 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 (43) was performed using ES-MS (direct infusion in water, Calculated [M+H]+=1973.8, Observed [M+H]+=1974.0)
Workup
- filtrationfiltered
- filtration2 mL×5 min), filtered
- washwashed (NMP)
- additionadded to the resin
- additionmixed for 30 min
- filtrationResin was then filtered
- washwashed with NMP
- additionadded to the resin
- washAfter 30 min resin was washed with NMP
- custom95:5 TFA-water (200 μL, 2 h)
- customprecipitated
Sources & evidence
- ORD record
- ord-444a886ddb6b49cebaef960a50dcdb6e
- Source dataset
- uspto-grants-2013_08
- Patent number
- US08501498B2
Reaction notes
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