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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2375484Generated: October 30, 2026

Benzaldehyde → HCID 58863836, compound

https://huagongshe.com/reaction/2375484

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 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 numberUS07465750B2
Source datasetuspto-grants-2008_12
ORD IDord-494ba0aeb7ce4d0cb7053d77e57dc112
Source noteuspto-grants-2008_12