Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 930315Generated: November 1, 2026

Toluene → HCID 78321448, compound

https://huagongshe.com/reaction/930315

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantLawesson's reagentHCID 87949—
ReactantHCID 86732142HCID 86732142—
SolventEthyl AcetateHCID 8857—
ProductHCID 78321448HCID 7832144812.2%

Reaction Conditions

Temperature120 °C

Reaction Steps

A sealable vial was charged with N-(3-((4S,6S)-2-amino-4-(fluoromethyl)-6-(trifluoromethyl)-5,6-dihydro-4H-1,3-oxazin-4-yl)-4-fluorophenyl)-5-chloro-3-methylpicolinamide (Example 4, 0.068 g, 0.147 mmol) and toluene (1 mL). 2,4-Bis(4-methoxyphenyl)-2,4-dithioxo-1,3,2,4-dithiadiphosphetane (0.059 g, 0.147 mmol) was added and the reaction mixture was heated to 120° C. overnight. Upon cooling to room temperature, the reaction mixture was taken up in EtOAc (75 mL). The organic layer was washed with aqueous saturated NaHCO3 and with brine, dried over MgSO4 and concentrated under reduced pressure. The residue was purified through silica gel (gradient 30%-50% EtOAc-hexane) affording the title compound as a yellow solid (8.4 mg, 0.018 mmol, 12%). MS m/z=479 [M+H]+. Calculated for C19H16ClF5N4OS: 478.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09296734B2
Source datasetuspto-grants-2016_03
ORD IDord-09be41b37b304c65a73a5683d181a40f
Source noteuspto-grants-2016_03