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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 973522Generated: October 29, 2026

4-Methylmorpholine → Boc-Ile-Pro-OBzl

https://huagongshe.com/reaction/973522

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
ReactantIsobutyl chloroformateHCID 62365—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantSodium BicarbonateHCID 516892—
Reactanttert-Butoxycarbonyl-L-isoleucineHCID 2724762—
ReactantProline benzyl ester hydrochlorideHCID 2733413—
SolventDimethylformamideHCID 6228—
ProductBoc-Ile-Pro-OBzlHCID 1430623592%

Reaction Conditions

Temperature-15 °C

Reaction Steps

Boc-Ile-OH (12.01 g, 0.05 mole) in DMF (50 ml) was cooled to 0° C. and NMM (5.49 ml) was added. After cooling the solution to -15° C. isobutylchloroformate (6.48 ml) was added slowly while maintaining the temperature at -15° C. and stirred for 10 minutes at which time HOBt (7.65 g) was added and stirring was continued for additional 10 minutes. A pre-cooled solution of HCl-H-Pro-OBzl (12.09 g, 0.05 mole) in DMF (50 ml) and NMN (5.49 ml) was added to the above solution and the completeness of the reaction was followed by TLC. The reaction mixture was poured into a cold saturated NaHCO3 solution and stirred for one hour. The peptide was extracted into CHCl3 and washed with acid and base (0.5 N NaOH to remove HOBt), and on evaporating the solvent the product was obtained as an 92% yield. Rf1, 0.65. Anal. Calcd. for C23H34N2O5 : C 66.00, H 9.19, N 6.69%. Found: C 65.58, H 8.28, N 7.13%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05064430
Source datasetuspto-grants-1991_11
ORD IDord-6aad5a2cf1c843bbb870535fd8f6f9ce
Source noteuspto-grants-1991_11