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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | Bromotrimethylsilane | HCID 76113 | — |
| Reactant | Diethyl[(6-bromo-2-cyanoquinolin-7-yl)(difluoro)methyl]phosphonate | HCID 86638326 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Diammonium[(6-bromo-2-cyanoquinolin-7-yl)(difluoro)methyl]phosphonate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09334295B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-9d819738468e46bb823119b1c93ca415 |
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| Source note | uspto-grants-2016_05 |
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