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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1591989Generated: November 1, 2026

N-Acetyl-L-phenylalanine → HCID 67139620, compound

https://huagongshe.com/reaction/1591989

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-Acetyl-L-phenylalanineHCID 74839—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantHCID 67138311HCID 67138311—
SolventDichloromethaneHCID 6344—
ProductHCID 67139620HCID 67139620—

Reaction Steps

HOBt (19 mg, 0.125 mmol), (S)-2-acetylamino-3-phenyl-propionic acid (26 mg, 0.125 mmol) and EDCl (26 mg, 0.138 mmol) are added to a solution of the title G compound, (S)-2-amino-3-{3-[5-(4-methoxy-benzyl)-1,1,4-trioxo-1,2,5-thiadiazolidin-2-ylmethyl]-phenyl}-N-pentylpropionamide (63 mg, 0.125 mmol) in CH2Cl2 (4 mL) at RT. After 30 min, the reaction is concentrated. The product is taken up in EtOAc, washed with 1N aqueous HCl, saturated aqueous NaHCO3 and brine. The organic solution is dried over anhydrous MgSO4 and concentrated to yield (S)-2-((S)-2-acetylamino-3-phenyl-propionylamino)-3-{3-[5-(4-methoxy-benzyl)-1,1,4-trioxo-1,2,5-thiadiazolidin-2-ylmethyl]-phenyl}-N-pentyl-propionamide as a white foam: [M+1]+=692.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07291635B2
Source datasetuspto-grants-2007_11
ORD IDord-9edac9711f7646c7b43bee1ed81085a4
Source noteuspto-grants-2007_11