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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 917301Generated: November 1, 2026

N-(3-Aminopropyl)morpholine → HCID 23625006, compound

https://huagongshe.com/reaction/917301

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(3-Aminopropyl)morpholineHCID 61055—
ReactantBoc-D-phenylalanineHCID 637610—
SolventTetrahydrofuranHCID 8028—
ProductHCID 23625006HCID 2362500691.1%

Reaction Steps

To a solution in 15 ml of anhydrous THF of tert-butyloxycarbonyl-D-phenylalanine N-hydroxysuccinimmidyl ester (500 mg, 1.38 mmol), N-(3-aminopropyl)-morpholine (1.328 mmol, 0.201 ml) is added. The stirring is maintained for 90 min. The solvent is then evaporated, and the residue dissolved with AcOEt (50 ml); the organic phase is washed with NaHCO3 1M (3×50 ml), HCl 1M (3×50 ml), saturated aqueous solution of sodium chloride (3×50 ml). The solution dried on anhydrous Na2SO4. Following the evaporation of the solvent, 474 mg of (ter-butyloxycarbonyl-D-phenylalanine-N-[3(morpholin-4-yl)propyl]amide) (1.21 mmol, yield=88%) are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07273856B2
Source datasetuspto-grants-2007_09
ORD IDord-fbe786b2eaee48e4bfe7e7c62f48ef21
Source noteuspto-grants-2007_09