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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 260248Generated: October 30, 2026

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

https://huagongshe.com/reaction/260248

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 4.2 N 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 rain, 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 filtered, washed with petroleum ether, and dried to obtain 76.2 g (yield 87.88%) of II. R1f 0.39; R2f, 0.44.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05527610
Source datasetuspto-grants-1996_06
ORD IDord-4bfb2ae552f84c4bb379337040a71e88
Source noteuspto-grants-1996_06