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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1655307Generated: October 31, 2026

4-Methylmorpholine → Boc-Ile-Pro-OBzl

https://huagongshe.com/reaction/1655307

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
ReactantIsobutyl chloroformateHCID 62365—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantSodium BicarbonateHCID 516892—
ReactantBenzyl L-prolinateHCID 736155—
Reactanttert-Butoxycarbonyl-L-isoleucineHCID 2724762—
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 NMM (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 (0.5N NaOH to remove HOBt), and on evaporting the solvent the product was obtained as an oil in 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 numberUS05250516
Source datasetuspto-grants-1993_10
ORD IDord-137e904c749d4aeba6f16a766e365b3d
Source noteuspto-grants-1993_10