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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1680566Generated: November 2, 2026

4-Methylmorpholine → HCID 70566328, compound

https://huagongshe.com/reaction/1680566

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
ReactantIsobutyl chloroformateHCID 62365—
ReactantN-(tert-Butyloxycarbonyl)-D-methionineHCID 111051—
ReactantHCID 70565612HCID 70565612—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 70566328HCID 70566328—

Reaction Steps

A mixed anhydride is prepared by reacting 2.0 g of Boc-D-methionine with 0.90 ml of N-methylmorpholine and 1.06 ml isobutylchloroformate in 15 ml of tetrahydrofuran at -20° C. A solution of 2.84 g of methyl glycyl-L-phenylalanyl-3-amino-1-adamantanecarboxylate hydrochloride in 15 ml tetrahydrofuran is neutralized with 0.78 ml N-methyl morpholine and added to the mixed anhydride reaction above. The reaction mixture is stirred for 2 hours at room temperature and allowed to stand overnight. The reaction mixture is diluted with 200 ml of ethyl acetate. The ethyl acetate layer is collected and washed with water, followed by washes with 0.2 M potassium bisulfate, water, and 1 M potassium bicarbonate and dried over magnesium sulfate. The solution is filtered and the solvent removed under reduced pressure. Purification of the residue by low pressure chromatography on silica gel affords methyl Boc-D-methionyl-glycyl-L-phenylalanyl-3-amino-1-adamantanecarboxylate which is represented by the following formula ##STR17##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04273704
Source datasetuspto-grants-1981_06
ORD IDord-fa350e6f18c44fa3ae7d19b80579269c
Source noteuspto-grants-1981_06