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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1352900Generated: November 2, 2026

Benzaldehyde → HCID 58863836, compound

https://huagongshe.com/reaction/1352900

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 68563369HCID 68563369—
SolventAcetic AcidHCID 176—
SolventMethanolHCID 887—
ProductHCID 58863836HCID 5886383640%

Reaction Steps

A mixture of N4-(3-methoxyphenyl)-N6,N6-dimethyl-2-(1-piperazinyl)-4,6-pyrimidinediamine (36 mg, 0.10 mmol) and benzaldehyde (11 mg, 0.1 mmol) in a solution of methanol (5 mL) and acetic acid (0.5 mL) was stirred at room temperature for 1 h. Sodium cyanoborohydride (7 mg, 0.1 mmol) was added to the above solution and stirred at room temperature for 16 h. The crude product was treated with saturated NaHCO3 (50 mL) and extracted with EtOAC (3×50 mL). The organic layer was washed with brine (2×50 mL), dried over Na2SO4, filtered, and concentrated in vacuo. The crude product was purified by chromatography on silica using hexane/EtOAc (1:3), giving the desired product (8 mg, 40%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07220775B2
Source datasetuspto-grants-2007_05
ORD IDord-2209c82ef7024b1e8b4b66bc7aa6ac2d
Source noteuspto-grants-2007_05