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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1524872Generated: October 25, 2026

L-Phenylalanine, N-[(1,1-dimethylethoxy)carbonyl]- → HCID 178513610, compound

https://huagongshe.com/reaction/1524872

Reaction equation

Participants

RoleNameHCIDCharge
ReactantL-Phenylalanine, N-[(1,1-dimethylethoxy)carbonyl]-HCID 77857—
Reactant4-(Bromoacetyl)benzonitrileHCID 98654—
ReactantBenzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphateHCID 151348—
ReactantCyano-2-(ethylamino)benzoic acidHCID 66674956—
SolventTetrahydrofuranHCID 8028—
SolventTriethylamineHCID 8471—
ProductHCID 178513610HCID 178513610—

Reaction Steps

Cyano-2-(ethylamino)benzoic acid from Example 140 Part C (40 mg, 0.2 mmol), Bop reagent (108 mg, 0.24 mmol), and Et3N (0.28 mL) were added together with 5 mL of THF. The mixture was stirred at RT for 15 minutes and (S)-4-(2-(1-Amino-2-phenylethyl)-1H-imidazol-4-yl)benzamide (107 mg, 0.2 mmol), obtained from N-boc-(L)-phenylalanine and 4-(2-Bromo-acetyl)-benzonitrile by the sequential application of the procedures described for Example 1 Part A, Example 28 Part A and Example 1 Part B, was added. The resulting mixture was heated to reflux under N2 for 2 h. The solvent were removed. The residue was dissolved in EtOAc and washed with water and brine. It was dried over MgSO4, concentrated, and purified by ISCO flash chromatography (silica, EtOAc/hexane) to give 50 mg of the desired product. LC/MS: 479.3 (M+1)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09079860B2
Source datasetuspto-grants-2015_07
ORD IDord-49e92c05695448c2af90dd9830491901
Source noteuspto-grants-2015_07