Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2252897Generated: October 30, 2026

Ammonium Chloride → HCID 59639533, compound

https://huagongshe.com/reaction/2252897

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant18-Crown-6HCID 28557—
ReactantNsc 634137HCID 184894—
ReactantPotassium bis(trimethylsilyl)amideHCID 3251421—
ReactantHCID 9856557HCID 9856557—
SolventTolueneHCID 1140—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
ProductHCID 59639533HCID 59639533108.8%

Reaction Steps

A solution of 18-crown-6 (422 mg, 1.6 mmol, 5 eq) and bis(2,2,2-trifluoroethyl) (methoxycarbonylmethyl)phosphonate (81 uL, 0.38 mmol, 1.2 eq) in anhyd THF (20 mL) was cooled to −78°, potassium bis(trimethylsilyl)amide (0.96 mL, 0.48 mmol, 1.5 eq) as a 0.5 mol solution in toluene was added. This solution was stirred for additional 30 min at −78° and 4-amino-6-(2-fluoro-phenyl)-2-methylsulfanyl-pyrimidine-5-carbaldehyde (85 mg, 0.32 mmol) in dry THF (1 mL) was added dropwise. The reaction mixture was then stirred for 8 h at −78° and warmed to 23°, and stirred 16 h. Saturated aq NH4Cl (5 mL), followed by Et2O (20 mL), was added. The layers were separated. The organic layer was washed with satd aq NaCl, dried (MgSO4), filtered and solvent was evaporated. The yellow residue was purified by Flash chromatography to afford 100 mg (91% yield) of 4-(2-fluoro-phenyl)-2-methylsulfanyl-8H-pyrido[2,3-d]pyrimidin-7-one. 1H-NMR δ 2.62 (s, 3H), 6.55 (d, 1H, J=9.9 Hz), 7.26 (m, 3H), 7.52 (m, 2H), 8.99 (br s, 1H). LC MS (m/e)=288 (MH+). Rt=1.75 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07323472B2
Source datasetuspto-grants-2008_01
ORD IDord-bb4e5643582d4b5ebb130aef8fe286ce
Source noteuspto-grants-2008_01