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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2293384Generated: October 31, 2026

Triethylamine → L-phenylalanine, N-[1-(2-adamantan-1-yl-2-oxoethyl)-L-prolyl] benzylamide

https://huagongshe.com/reaction/2293384

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantPhenylalanine benzylamideHCID 770095—
Reactant1-(2-adamantan-1-yl-2-oxoethyl) L-prolineHCID 54229701—
SolventDichloromethaneHCID 6344—
ProductL-phenylalanine, N-[1-(2-adamantan-1-yl-2-oxoethyl)-L-prolyl] benzylamideHCID 6762039480.3%

Reaction Conditions

Temperature22 °C

Reaction Steps

Using the procedure described previously, a solution of 1-(2-adamantan-1-yl-2-oxoethyl) L-proline (100 mg, 0.34 mmol, 1.0 eq), L-phenylalanine N-benzylamide (175 mg, 686 umol, 2.0 eq) and dichloromethane (1.0 mL), was cooled to 0° C., and treated with triethylamine (286 uL, 2.0 mmol, 6.0 eq). To this chilled solution was added a 50% solution of 1-n-propylphosphonic acid cyclic anhydride in dichloromethane (436 uL, 0.68 mL, 2.0 eq). When TLC indicated the reaction was complete, the solution was allowed to warm to 22° C., washed with satd aq NaHCO3, concentrated in vacuo, and purified by flash chromatography to provide 144 mg (80%) of L-phenylalanine, N-[1-(2-adamantan-1-yl-2-oxoethyl)-L-prolyl] benzylamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05686424
Source datasetuspto-grants-1997_11
ORD IDord-d3c7d422d58641d7ae7e946754ee7b83
Source noteuspto-grants-1997_11