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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2297581Generated: October 30, 2026

Formate → HCID 178425605, compound

https://huagongshe.com/reaction/2297581

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 numberUS06492372B1
Source datasetuspto-grants-2002_12
ORD IDord-d07414028e1048c088b1c81d9e917f8e
Source noteuspto-grants-2002_12