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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 369737Generated: October 30, 2026

Pyridine → HCID 54164588, compound

https://huagongshe.com/reaction/369737

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantDiethyl EtherHCID 3283—
ReactantBromoacetyl bromideHCID 61147—
ReactantHCID 69959296HCID 69959296—
ProductHCID 54164588HCID 54164588—

Reaction Steps

To a stirred 0° solution of 210 mg of 6-Amino-3-fluoro-α-isopropylethynyl-α-(trifluoromEthyl)benzyl alcohol in 20 mL of dry ether was added 120 mL of dry pyridine and 0.080 mL of bromoacetyl bromide. After 30 min, the reaction mixture was diluted with ether, washed with water and aqueous sodium bicarbonate, dried and evaporated. The residue was dissolved in 20 mL of dry DMF and was treated at room temperature with 33 mg of 100% sodium hydride for 30 min. The reaction was partitioned between ethyl acetate and water and the ethyl acetate layer was washed with brine, dried and evaporated. The crude product was purified by column chromatography over silica gel (elution with ethyl acetate/hexanes 1:2) affording after crystallization from ethyl acetate/hexanes 89 mg of the title compound as colorless crystals: mp 172-173°; Anal. Calcd. for C15H13NO2F4 : C, 57.15; H, 4.17; N, 4.44. Found: C, 57.10; H, 3.98; N, 4.21.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06140320
Source datasetuspto-grants-2000_10
ORD IDord-e3de1fde1cb546a0955d66bed314b416
Source noteuspto-grants-2000_10