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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1111310Generated: November 2, 2026

4-Methylmorpholine → HCID 18642403, compound

https://huagongshe.com/reaction/1111310

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
ReactantIsobutyl chloroformateHCID 62365—
ReactantBenzyloxycarbonyl-L-prolineHCID 101987—
ReactantHCID 22152159HCID 22152159—
SolventTetrahydrofuranHCID 8028—
ProductHCID 18642403HCID 18642403—

Reaction Conditions

Temperature-15 °C

Reaction Steps

A solution was prepared by dissolving 249 mg of N-carbobenzoxy-L-proline and 101.0 mg of N-methylmorpholine in 5 ml of dry tetrahydrofuran and cooling to a temperature of -15° C. The solution was mixed with 136.6 mg of isobutyl chloroformate and the mixture was stirred at a temperature of -15° C. to -10° C. for 2 minutes. Then, a solution of 238 mg of 4-amino-2-carboisopropoxyaminobenzoic acid and 101.2 mg of N-methylmorpholine in 2 ml of dry tetrahydrofuran was added dropwise to the above-mentioned mixture. The resultant reaction mixture was stirred at a temperature of -15° C. to -10° C. for one hour, gradually heated to room temperature, and then stirred at room temperature for 18 hours. The resultant deposit generated in the reaction mixture was removed by filtration, the filtrate was concentrated under a reduced pressure, and an oily yellow substance was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04980287
Source datasetuspto-grants-1990_12
ORD IDord-a7054b498dba4f389f580038aa0fa1ed
Source noteuspto-grants-1990_12