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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1395813Generated: October 30, 2026

4-Methylmorpholine → HCID 178501375, compound

https://huagongshe.com/reaction/1395813

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
ReactantIsobutyl chloroformateHCID 62365—
ReactantGlycine, N-[(1,1-dimethylethoxy)carbonyl]-N-methyl-HCID 83692—
ReactantHCID 178501377HCID 178501377—
SolventDichloromethaneHCID 6344—
ProductHCID 178501375HCID 178501375—

Reaction Conditions

Temperature-70 °C

Reaction Steps

8.84 g of t-butoxycarbonylsarcosine is dissolved in 200 ml of methylene chloride. 10.5 ml of N-methylmorpholine is added to the solution. The solution is cooled to -70° C. 6.1 ml of isobutyl chloroformate is then added. The reaction mixture is warmed up to -15° C. and stirred for 5 minutes. The reaction mixture is again cooled to -70° C. 25.5 g of nitroarginylvalyltyrosine methyl ester hydrochloride is added to the reaction mixture. The reaction mixture is allowed to warm to room temperature, and then is stirred for 16 hours. The reaction mixture is extracted three times with 0.5 M potassium bisulfate and once with brine. The methylene chloride solution is dried over anhydrous sodium sulfate, filtered and stripped of solvent. The residue is dissolved in 200 ml of ethyl ether. The ether solution is added to cold rapidly stirring Skellysolve B. The white precipitate is filtered and dried to afford the product t-butoxycarbonylsarcosylnitroarginylvalyltyrosine methyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04204991
Source datasetuspto-grants-1980_05
ORD IDord-1032476ff95445a4b3070184f5257448
Source noteuspto-grants-1980_05