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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 613835Generated: October 30, 2026

Triethylamine → HCID 178472546, compound

https://huagongshe.com/reaction/613835

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantHCID 3481676HCID 3481676—
ReactantHCID 178472566HCID 178472566—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178472546HCID 17847254619.8%

Reaction Steps

A solution of 0.5 g (1.5 mmol) of bis-(1-naphthylmethyl)-acetic acid, 0.77 g (3.0 mmol) of histidine ethyl ester dihydrochloride (His-OEt·2 HCl), and 0.22 g (1.6 mmol) of 1-hydroxybenzotriazole (HOBt) in 20 mL of THF was treated with 0.85 mL (6.0 mmol) of Et3N followed by 0.33 g (1.6 mmol) of N,N'-dicyclo hexylcarbodiimide (DCC) and the solution allowed to stir at room temperature overnight. The mixture was filtered and the solvent removed under reduced pressure. The residue was taken up in EtOAc and washed with a saturated solution of NaHCO3, then with a saturated solution of NaCl. Drying over MgSO4 and removal of the solvent under reduced pressure gave the crude product. Chromatography on silica gel, eluting with a gradient of methylene chloride (CH2Cl2) to CH2Cl2 /MeOH (96/4) gave 0.15 g of the product as a white foam. The structure was confirmed by NMR and mass spectroscopy; (m+H)+ =506.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06008372
Source datasetuspto-grants-1999_12
ORD IDord-e99207dcf528419bb620979119c4f291
Source noteuspto-grants-1999_12