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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 369742Generated: October 31, 2026

Pyridine → HCID 18387394, compound

https://huagongshe.com/reaction/369742

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantBromoacetyl bromideHCID 61147—
Reactant6-Amino-2,3-difluoro-alpha-(isopropylethynyl)-alpha-(trifluoromethyl)benzyl alcoholHCID 54375021—
SolventDiethyl EtherHCID 3283—
ProductHCID 18387394HCID 18387394—

Reaction Steps

To a stirred ice-cooled soliution of 81 mg of 6-Amino-2,3-difluoro-α-(isopropylethynyl)-α-(trifluoromethyl)benzyl alcohol in 8 mL of dry ether was added 0.55 mL of dry pyridine and 0.032 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 10 mL of dry DMF and was treated at 0° with 10 mg of 100% sodium hydride for 20 min. The cooling bath was removed, and the reaction was allowed to proceed at ambient temperature for 1 h. The reaction was quenched with one drop of acetic acid and then the mixture was concentrated in vacuo. The residue was dissolved in ethyl acetate and this solution vas washed with water and brine, dried and evaporated to a solid which was crystallized from ethyl acetate/hexanes affording 28 mg of the title compound as colorless crystals: mp 192.5-193.5°; HRMS: Calcd. for C15H13NO2F5 (M+H)+ : 334.086645. Found: 334.084917.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06140320
Source datasetuspto-grants-2000_10
ORD IDord-3430fb3b9f974004bdf52016cef54d99
Source noteuspto-grants-2000_10