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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 440230Generated: October 30, 2026

4-Methylmorpholine → Boc-Gly-Ala-Pro-OBzl

https://huagongshe.com/reaction/440230

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantN-(tert-butoxycarbonyl)glycineHCID 78288—
ReactantN-[(1,1-Dimethylethoxy)carbonyl]-L-alanyl-L-proline phenylmethyl esterHCID 13068139—
SolventHydrochloric AcidHCID 313—
SolventDimethylformamideHCID 6228—
Solvent1,4-DioxaneHCID 31275—
ProductBoc-Gly-Ala-Pro-OBzlHCID 1465648687.9%

Reaction Steps

Boc-Ala-Pro-OBzl (75.3 g, 0.2 mole) was deprotected by stirring for 1.5 h. in 4.2N HCl in dioxane. Excess HCl and dioxane were removed under reduced pressure, triturated with ether, faltered, washed with ether, and dried (yield 100%). A solution of Boc-Gly-OH (35.04 g, 0.2 mole) and HOBt (27.02 g, 0.2 mole) in DMF was cooled to -15° C. with stirring and EDCI (38.34 g, 0.2 mole) was added. After 20 min, a pre-cooled solution containing the above hydrochloride salt and NMM (21.98 mL, 0.2 mole) was added and the reaction mixture was stirred overnight at room temperature. The mixture was evaporated to a thick oil which was dissolved in CHCl3. This solution was extracted with water, 10% citric acid, water, 5% NaHCO3, water, and dried over Na2SO4. The solvent was removed under reduced pressure and the resulting oil was crystallized from ether/petroleum ether. The solid was faltered, washed with petroleum ether, and dried to obtain 76.2 g (yield 87.88%) of II. Rf1 0.39; Rf2, 0.44.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05519004
Source datasetuspto-grants-1996_05
ORD IDord-9e0c40185341460cb1cf9e477839d785
Source noteuspto-grants-1996_05