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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2063331Generated: November 2, 2026

Ethyl Acetate → HCID 44513518, compound

https://huagongshe.com/reaction/2063331

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantSodium BicarbonateHCID 516892—
ReactantHydrogen chloride-ethyl acetateHCID 21866389—
ReactantHCID 67049699HCID 67049699—
SolventMethanolHCID 887—
SolventChloroformHCID 6212—
ProductHCID 44513518HCID 4451351877%

Reaction Steps

4.0M Hydrogen chloride-ethyl acetate solution (5.0 mL) was added to a solution of N-(4-t-butoxycarbonylaminothiophen-3-yl)-5-[3-(2,3-dihydrobenzo[1,4]dioxin-6-yl)-1-(2-dimethylaminoethyl)ureidomethyl]pyridine-2-carboxylic acid amide (Reference Compound No. 6-4, 60 mg, 0.10 mmol) in a mixed solvent of ethyl acetate (2.0 ml)—methanol (3.0 mL), and then the reaction mixture was stirred at room temperature for 2 hours. Chloroform (0.10 L) and saturated aqueous sodium hydrogen carbonate solution (0.15 L) were added to a reaction solution, and then the whole was partitioned. The organic layer was washed with brine (0.10 L). The organic layer was dried over anhydrous magnesium sulfate and the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography (chloroform-methanol) to give 38 mg of the title compound as an orange amorphous product. (Yield 77%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08288380B2
Source datasetuspto-grants-2012_10
ORD IDord-7bd717b29b124012b1052017dfd000a1
Source noteuspto-grants-2012_10