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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1162946Generated: October 29, 2026

Triethylamine → HCID 57558028, compound

https://huagongshe.com/reaction/1162946

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantAmmonium ChlorideHCID 25517—
ReactantEthyl isocyanatoacetateHCID 76283—
ReactantHCID 11668552HCID 11668552—
SolventDichloromethaneHCID 6344—
ProductHCID 57558028HCID 5755802892%

Reaction Steps

Ethyl isocyanatoacetate (6.6 μL, 0.059 mmol) and triethylamine (10.3 μL, 0.074 mmol) were added to a solution of 7-((R)-5-hydroxymethyl-2-oxooxazolidin-3-yl)-3-(2-trifluoromethylphenyl)-2H-isoquinolin-1-one obtained in Step B of Example 1-14 (20 mg, 0.050 mmol) in dichloromethane, and the mixture was stirred at room temperature for four hours. Aqueous saturated ammonium chloride was added to the mixture, followed by extraction with dichloromethane. The extract was dried over anhydrous sodium sulfate, and then the solvent was evaporated under reduced pressure. The resulting residue was purified by aminosilica gel column chromatography (methylene chloride:methanol=50:1) to obtain 24 mg (92%) of ethyl{(R)-2-oxo-3-[1-oxo-3-(2-trifluoromethylphenyl)-1,2-dihydroisoquinolin-7-yl]oxazolidin-5-ylmethoxycarbonylamino}acetate as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07820693B2
Source datasetuspto-grants-2010_10
ORD IDord-1aee97fd4def4299a15530ba0a831f05
Source noteuspto-grants-2010_10