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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1008953Generated: October 26, 2026

Formate → HCID 178425605, compound

https://huagongshe.com/reaction/1008953

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormateHCID 283—
ReactantTriethylamineHCID 8471—
Reactant2-(3-Methylphenylaminocarbonylamino)eth-1-ylamineHCID 22138859—
ReactantHCID 178467516HCID 178467516—
SolventEthanolHCID 702—
ProductHCID 178425605HCID 17842560591%

Reaction Steps

To a solution of N-(4-ethoxy-1,1-dioxo-1,2,5-thiadiazol-3-yl)-L-tyrosine tert-butyl ester from Step A (150 mg, 0.38 mmol) and the formate salt of 2-(3-methylphenylaminocarbonylamino)eth-1-ylamine from Step B (210 mg, 0.89 mmol) in ethanol (10 mL) was added triethylamine (133 mg, 1.44 mmol). The reaction was stirred at room temperature overnight. Solvent was removed under reduced pressure and the residue purified by flash column chromatography (silica, 5% MeOH in EtOAc) to give the title compound (130 mg, 91%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07973044B2
Source datasetuspto-grants-2011_07
ORD IDord-b1c6f4c7a50e4df7a9d486915c47d30b
Source noteuspto-grants-2011_07