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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 341500Generated: October 31, 2026

Water → 1-[6-(3-{4-Amino-6-[methyl(phenyl)amino]-1,3,5-triazin-2-yl]-1,2,4-oxadiazol-5-yl)pyridin-3-yl}ethan-1-ol

https://huagongshe.com/reaction/341500

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantEthyl AcetateHCID 8857—
ReactantSodium borohydrideHCID 4311764—
Reactant1-[6-(3-{4-Amino-6-[methyl(phenyl)amino]-1,3,5-triazin-2-yl}-1,2,4-oxadiazol-5-yl)pyridin-3-yl]ethan-1-oneHCID 66802627—
SolventTetrahydrofuranHCID 8028—
Product1-[6-(3-{4-Amino-6-[methyl(phenyl)amino]-1,3,5-triazin-2-yl]-1,2,4-oxadiazol-5-yl)pyridin-3-yl}ethan-1-olHCID 66803195106.7%

Reaction Steps

1-[6-(3-{4-Amino-6-[methyl(phenyl)amino]-1,3,5-triazin-2-yl}-1,2,4-oxadiazol-5-yl)pyridin-3-yl]ethan-1-one (Intermediate 141, 0.934 g, 2.40 mmol) was suspended in THF (60 mL), sodium borohydride (0.227 g, 6.01 mmol) was added and the mixture stirred at room temperature for 2 h. EtOAc (50 mL) and water (100 mL) were added and the organic layer separated. The aqueous layer was neutralised using 1M aq. hydrochloric acid and extracted with EtOAc (3×30 mL). The combined organic layers were dried over sodium sulfate and concentrated under vacuum to afford the title compound as a pale yellow solid (1.0 g), which was used in the next step without further purification. Method C HPLC-MS: MH+ requires m/z=391 Found: m/z=391, Rt=1.18 min (84%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08895733B2
Source datasetuspto-grants-2014_11
ORD IDord-e1c13c80164a46d58265cc21823a951c
Source noteuspto-grants-2014_11