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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1418419Generated: November 2, 2026

4-Methylmorpholine → HCID 131720087, compound

https://huagongshe.com/reaction/1418419

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantProline benzyl ester hydrochlorideHCID 2733413—
ReactantBoc-Met(O2)-OHHCID 7017894—
SolventDichloromethaneHCID 6344—
ProductHCID 131720087HCID 131720087—

Reaction Steps

N-Boc-L-methionine sulfone-L-proline-O-benzyl ester was prepared by adding to a solution of N-Boc-L-methionine sulfone (14.0 g, 50.0 mmole) in dichloromethane (150 mL) at 0° C., HOBt (10.1 g, 75 mmole) followed by DCC (11.33 g, 55.0 mmole). The mixture was stirred for 10 minutes, and then L-proline benzyl ester hydrochloride salt (50.0 mmole, 12.0 g) was added followed by NMM (100 mmole, 10.9 mL). The resulting mixture was stirred in an ice bath and allowed to come to room temperature over 12 hours. The mixture was filtered to remove dicyclohexylurea and ethyl acetate (300 mL) was added. The organic phase was then added to a separatory funnel and washed with saturated aqueous sodium bicarbonate, brine and then 1M aqueous HCl. The organic phase was dried over magnesium sulfate and then filtered. The organic phase was then reduced on a rotary evaporator under vacuum and then on a high vacuum line to remove traces of solvent to provide 23.5 g of a white solid (100%). Rf=0.34 (silica, 5:95 methanol/chloroform).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05883107
Source datasetuspto-grants-1999_03
ORD IDord-16e92469f9324c4b93cebc86cbf7115d
Source noteuspto-grants-1999_03