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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 526772Generated: October 27, 2026

Water → HCID 117666121, compound

https://huagongshe.com/reaction/526772

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantN-Benzyl-N,N'-dimethylethylenediamineHCID 66016—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 43324280HCID 43324280—
CatalystZincchlorideHCID 3007855—
SolventMethanolHCID 887—
ProductHCID 117666121HCID 11766612147.7%

Reaction Steps

To a solution of 3-(4-isopropoxyphenyl)-1-methyl-1H-pyrazole-4-carbaldehyde (82 mg, 0.32 mmol) in methanol (2 mL) was added TEA (129 mg, 1.2 mmol). ZnCl2 (5 mg, 0.05 mmol) and N-benzyl-N,N′-dimethylethane-1,2-diamine (71 mg, 0.38 mmol) were added at rt and stirred for 45 min. NaCNBH3 (87 mg, 1.2 mmol) was added and stirred for 2 h at rt. The reaction was poured into water (100 mL), extracted with EtOAc (50 mL×2). The combined extracts was washed with brine (100 mL), dried and concentrated under vacuum. The residue was purified by SGC using DCM: MeOH (0%-4%) as eluent to obtain N1-benzyl-N2-((3-(4-isopropoxyphenyl)-1-methyl-1H-pyrazol-4-yl)methyl)-N1,N2-dimethylethane-1,2-diamine (62 mg, Yield: 45%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09346761B2
Source datasetuspto-grants-2016_05
ORD IDord-5ef8280224db48e1b974d694d0545469
Source noteuspto-grants-2016_05