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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 537041Generated: October 30, 2026

Hydrazine → HCID 178474055, compound

https://huagongshe.com/reaction/537041

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazineHCID 9321—
ReactantDimethylformamide dimethyl acetalHCID 78373—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 56839570HCID 56839570—
SolventTolueneHCID 1140—
ProductHCID 178474055HCID 17847405545%

Reaction Conditions

Temperature50 °C

Reaction Steps

A suspension of 2-[2-(acetylamino)-5-methylpyridin-4-yl]-5-(2-chlorophenyl)-1,3-oxazole-4-carboxamide (0.48 g, 1.3 mmol) in dry toluene (7 mL) was sonicated for 15 min. DMF-DMA (0.51 mL, 3.8 mmol) was added and the mixture was allowed to stir at 50° C. for 2 h. The suspension was cooled to rt and was concentrated. The resulting solid was suspended in AcOH (5 mL) at rt. Hydrazine (0.20 mL, 6.4 mmol) was added dropwise. The reaction mixture was allowed to stir at 40° C. for 3 h. Saturated NaHCO3 was added until the mixture became neutral. The solid was filtered, washed with water, and purified by column chromatography to give N-{4-[5-(2-chlorophenyl)-4-(4H-1,2,4-triazol-3-yl)-1,3-oxazol-2-yl]-5-methylpyridin-2-yl}acetamide (0.23 g, 45%). LCMS (FA): m/z=395.3 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08859768B2
Source datasetuspto-grants-2014_10
ORD IDord-f1447045ece54a8dab4c6a5120a15e99
Source noteuspto-grants-2014_10