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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 930439Generated: October 29, 2026

Ethyl Acetate → HCID 86732276, compound

https://huagongshe.com/reaction/930439

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantPropylphosphonic anhydrideHCID 111923—
Reactant5-Chloro-2-picolinic acidHCID 2762872—
ReactantHCID 86732275HCID 86732275—
SolventDimethylformamideHCID 6228—
ProductHCID 86732276HCID 8673227623.4%

Reaction Steps

To a mixture of (4S,6S)-4-(5-amino-2-chloro-3-fluorophenyl)-4-methyl-6-(trifluoromethyl)-5,6-dihydro-4H-1,3-oxazin-2-amine (0.060 g, 0.184 mmol) and 5-chloropicolinic acid (0.035 g, 0.221 mmol) in DMF (1.5 mL) at 0° C. was added 1-propanephosphonic acid cyclic anhydride, 50% solution in ethyl acetate (0.130 mL, 0.221 mmol). The reaction was gradually warmed to rt and stirred for 2 h. The reaction mixture was partitioned between EtOAc and saturated solution of NaHCO3. The organic layer was separated, washed twice with water, then washed with brine, dried over MgSO4, filtered, and concentrated in vacuo. The crude was purified by flash chromatography on silica gel (12 g, 0-100% EtOAc/DCM in 15 min). The fractions were combined and concentrated in vacuo. The resulting white solid was dissolved in MeOH and purified by reverse phase prep HPLC: 10-80% MeCH in Water (with 0.1% TFA). The fractions were collected and neutralized with solid Na2CO3, extracted with DCM three times. The organic solution was dried over sodium sulfate and concentrated in vacuo to give N-(3-((4S,6S)-2-amino-4-methyl-6-(trifluoromethyl)-5,6-dihydro-4H-1,3-oxazin-4-yl)-4-chloro-5-fluorophenyl)-5-chloropicolinamide (20 mg, 23.3% yield). MS m/z=465 [M+H]+. Calculated for C18H14Cl2F4N4O2: 465.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09296734B2
Source datasetuspto-grants-2016_03
ORD IDord-34ad79c5d99f4d75a8fa5f4e3c91a4bf
Source noteuspto-grants-2016_03