Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 523133Generated: October 30, 2026

Ammonia → Diammonium[(6-bromo-2-cyanoquinolin-7-yl)(difluoro)methyl]phosphonate

https://huagongshe.com/reaction/523133

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantMethanolHCID 887—
ReactantBromotrimethylsilaneHCID 76113—
ReactantDiethyl[(6-bromo-2-cyanoquinolin-7-yl)(difluoro)methyl]phosphonateHCID 86638326—
SolventDichloromethaneHCID 6344—
ProductDiammonium[(6-bromo-2-cyanoquinolin-7-yl)(difluoro)methyl]phosphonateHCID 67501574—

Reaction Steps

To a stirred solution of diethyl[(6-bromo-2-cyanoquinolin-7-yl)(difluoro)methyl]phosphonate (370 mg, 0.883 mmol) in dichloromethane (9) at 0° C. was added dropwise bromotrimethylsilane (1.15 mL, 8.83 mmol). The reaction mixture was stirred at room temperature overnight. It was concentrated to dryness, and co-evaporated with dichloromethane (2×). Ethanol (5 mL) was added to the residue, which was stirred for 20 minutes. It was concentrated to dryness and co-evaporated with ethanol (2×). The residue was dissolved in methanol (8 mL) and 2.0 M ammonia in methanol (4.4 mL, 8.80 mmol) was added dropwise. It was stirred for 20 minutes, concentrated to dryness and suspended in diethyl ether. The precipitate was filtered to afford diammonium[(6-bromo-2-cyanoquinolin-7-yl)(difluoro)methyl]phosphonate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09334295B2
Source datasetuspto-grants-2016_05
ORD IDord-9d819738468e46bb823119b1c93ca415
Source noteuspto-grants-2016_05