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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1599039Generated: October 31, 2026

Picolinic acid → HCID 18381987, compound

https://huagongshe.com/reaction/1599039

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 mL (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 1 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 4M HCl and diluted with methylene chloride. The aqueous layer was basified with 1N 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 numberUS05739135
Source datasetuspto-grants-1998_04
ORD IDord-49c4048ed05f4262916bfe453b9a16f8
Source noteuspto-grants-1998_04