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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2297533Generated: October 29, 2026

Picolinic acid → HCID 18381987, compound

https://huagongshe.com/reaction/2297533

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPicolinic acidHCID 1018—
ReactantTriethylamineHCID 8471—
ReactantBis(2-oxo-3-oxazolidinyl)phosphinic chlorideHCID 152842—
ReactantHCID 131720602HCID 131720602—
SolventDichloromethaneHCID 6344—
ProductHCID 18381987HCID 1838198785.6%

Reaction Steps

To a stirred suspension of 199 mg (1.62 mmol) of picolinic acid in 2.5 mL of methylene chloride at 0° C. was added 225 μL (1.62 mmol) of triethylamine. After all the solids had dissolved, the solution was treated with 412 mg (1.62 mmol) of bis(2-oxo-3-oxazolidinyl)phosphinic chloride, and stirred for 30 minutes. A methylene chloride solution of 535 mg (1.62 mmol) of compound E from Example 10 was converted to the free amine by washing with sodium bicarbonate and concentrating the organic layer to a brown oil which was redissolved in 1 mL of dry methylene chloride and added to the reaction mixture. After stirring at room temperature for 16 hours, the reaction was quenched with water and 4 M HCl and diluted with methylene chloride. The aqueous layer was basified with 1 N KOH and extracted two times. The combined organics were dried (sodium sulfate) and concentrated to provide 554 mg of a brown oil. The crude product was purified by flash chromatography on silica gel eluted with 98:2 ethyl acetate/methanol to provide 316 mg (58%) of compound A as a brown glass.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06492365B1
Source datasetuspto-grants-2002_12
ORD IDord-4a055eb622a34b3cb03272e06350af00
Source noteuspto-grants-2002_12