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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1970883Generated: November 2, 2026

Dichloromethane → {3-[5-(4-Methylpiperazin-1-yl)pyrimidin-2-yl]phenyl}methanol

https://huagongshe.com/reaction/1970883

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantSodium SulfateHCID 24436—
ReactantDiisobutylaluminumhydrideHCID 21225700—
ReactantMethyl 3-[5-(4-methylpiperazin-1-yl)pyrimidin-2-yl]-benzoateHCID 59484904—
SolventTetrahydrofuranHCID 8028—
Product{3-[5-(4-Methylpiperazin-1-yl)pyrimidin-2-yl]phenyl}methanolHCID 59484860—

Reaction Steps

860 mg (2.75 mmol) of methyl 3-[5-(4-methylpiperazin-1-yl)pyrimidin-2-yl]-benzoate are dissolved in 16 ml of THF, and 13.8 ml (13.8 mmol) of 1 M diisobutylaluminium hydride in THF are added dropwise at room temperature, and the reaction mixture is stirred at room temperature for 1 h. A further 13.8 ml (13.8 mmol) of 1 M diisobutylaluminium hydride in THF are added dropwise, and the reaction mixture is stirred at room temperature for 1 h. 3 ml of saturated sodium sulfate solution are added to the reaction mixture with ice cooling. Dichloromethane is added to the gelatinous mixture, which is then stirred for 30 min and filtered. The filtrate is dried over sodium sulfate and evaporated. Yield: 300 mg, yellow solid. The product is reacted further without further purification; HPLC: 1.68 min (method B); ESI: 285 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08431572B2
Source datasetuspto-grants-2013_04
ORD IDord-c59b85c11c7548708639c101261139e7
Source noteuspto-grants-2013_04