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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2172173Generated: October 30, 2026

L-Glutamine → HCID 13819651, compound

https://huagongshe.com/reaction/2172173

Reaction equation

Participants

RoleNameHCIDCharge
ReactantL-GlutamineHCID 5961—
ReactantSodium BicarbonateHCID 516892—
ReactantL-Valine, N-((phenylmethoxy)carbonyl)-, 2,5-dioxo-1-pyrrolidinyl esterHCID 853556—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
ProductHCID 13819651HCID 13819651—

Reaction Conditions

Temperature5 °C

Reaction Steps

H-Gln-OH (2 eq.) and NaHCO3 (2 eq.) were dissolved under stirring in water at maximum 45° C. and then cooled to about 5° C. Z-Val-OSu (1 eq.) was dissolved in MeCN and added in the aqueous solution in such way that the temperature did not rise above 10° C. The mixture was stirred for at least 1 h at ±5° C. before being warmed to room temperature for at least two hours. The peptide solution was concentrated under vacuum, diluted with water and washed twice with AcOEt. The aqueous phase was then diluted with i-BuOH and the pH was adjusted to 2.5 with a solution of KHSO4. DCM was then added to extract the peptide into the organic phase which was washed with a 5% weight NaCl solution and finally with water. The organic phase was collected and concentrated under reduced pressure until water content in the evaporates was <1% weight. The concentrate was diluted with hot isopropyl acetate and left to cool to 25° C. under gentle stirring to crystallize the peptide. The solid was recovered by filtration, once washed with AcOiPr at 25° C. and dried under vacuum until AcOiPr content in the peptide was ≦5% weight. After drying under vacuum not less than 70% of Z-Val-Gln-OH was recovered.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09051349B2
Source datasetuspto-grants-2015_06
ORD IDord-c543d728a7fd4d0ca6cecae312c5d147
Source noteuspto-grants-2015_06