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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2426100Generated: November 3, 2026

Formate → HCID 178425605, compound

https://huagongshe.com/reaction/2426100

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 numberUS07968547B2
Source datasetuspto-grants-2011_06
ORD IDord-50967b540ac0417ea84484251f6b5998
Source noteuspto-grants-2011_06