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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 411266Generated: October 27, 2026

4-Methylmorpholine → N-(Toluene-4-sulfonyl)-L-alanyl-L-phenylalanine Benzyl Ester

https://huagongshe.com/reaction/411266

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
ReactantBenzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphateHCID 151348—
ReactantBenzyl 3-phenyl-L-alaninateHCID 736312—
ReactantN-Tosyl-L-alanineHCID 737622—
SolventDimethylformamideHCID 6228—
ProductN-(Toluene-4-sulfonyl)-L-alanyl-L-phenylalanine Benzyl EsterHCID 5393799240.3%

Reaction Steps

To N-(toluene-4-sulfonyl)-L-alanine (2.0 mmoles) in DMF (10 mL) was added BOP (2.1 mmoles) and N-methylmorpholine (4.0 mmoles) and the reaction stirred at room temperature for 45 minutes. L-Phenylalanine benzyl ester (2.0 mmoles) was added and the reaction stirred for 16 hours at room temperature. The reaction mixture was extracted with water (100 mL) and diethyl ether (3×50 mL) The combined organic layers were successively washed with 0.2 N HCl (2×50 mL), sat. NaHCO3 (50 mL), and sat. NaCl (50 mL). The organic layer was dried over MgSO4, filtered, and concentrated to yield a colorless oil (387 mg, 40%). The crude product was purified by silica gel chromatography (50% EtOAc /Hexane, Rf=0.61). The title compound was crystalized from CHCl3/Hexane to yield a white solid, mp=109-110° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06559127B1
Source datasetuspto-grants-2003_05
ORD IDord-ad725e2be6674f7db449e0af3efe9b03
Source noteuspto-grants-2003_05