HCID 131721711, compound → L-Glutamine
Reaction equation
[NH2:1][C@H:2]([C:8]([OH:10])=[O:9])[CH2:3][CH2:4][C:5](=[O:7])[NH2:6].CC[C@@H]([C@H]1NC(=O)[C@@H](NC([C@H](NC)CC(C)C)=O)[C@@H](C)OC(=O)[C@H](CC2C=CC(OC)=CC=2)N(C)C(=O)[C@H]2N(CCC2)C(=O)[C@H](CC(C)C)NC(=O)[C@@H](C)C(=O)[C@H](C(C)C)OC(=O)C[C@@H]1O)C>C(O)(C)C.[Pd]>[NH2:1][C@H:2]([C:8]([OH:10])=[O:9])[CH2:3][CH2:4][C:5](=[O:7])[NH2:6]Participants
4
Reactant 1
Product 1
Reagents, catalysts & solvents 2
Procedure
The protected form of L-Gln-didemnin A (3.20 mg, 2.60 umol) was dissolved in isopropyl alcohol (0.50 mL) and 10% Pd/C catalyst (3.00 mg) was added. The solution was hydrogenated for 3 h, then the catalyst was removed by filtration over celite and solvent was removed to afford L-Gln-DA (2.30 mg, 88%); FABMS 1071.5 (M+H); HRFABMS Calcd for C54H87N8O14 (M+H) 1071.6341, Found 1071.6342.
Workup
- customthe catalyst was removed by filtration over celite and solvent
- customwas removed
Sources & evidence
- ORD record
- ord-5eb3c2e253de4bafb8a7eac35c66096a
- Source dataset
- uspto-grants-2000_03
- Patent number
- US06034058
Reaction notes
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