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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1422585Generated: November 1, 2026

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

https://huagongshe.com/reaction/1422585

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 numberUS08927526B2
Source datasetuspto-grants-2015_01
ORD IDord-1cdb1480de7043a7a49e14a8cc2f6609
Source noteuspto-grants-2015_01