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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1618112Generated: October 31, 2026

Dichloromethane → HCID 49873225, compound

https://huagongshe.com/reaction/1618112

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 49873315HCID 49873315—
SolventMethanolHCID 887—
ProductHCID 49873225HCID 49873225—

Reaction Steps

To a suspension of 1-methyl-3-oxo-2-(piperidin-4-yl)-2,3-dihydro-1H-isoindole-4-carboxamide (60 mg, 0.19 mmol) in dichloromethane (2 mL) cyclohexanone (147 mg, 0.28 mmol) sodium acetate (32 mg, 0.38 mmol) and methanol (0.3 mL) were added. The resulted solution was stirred at room temperature for 5 hours. Then sodium cyanoborohydride was added and the mixture was stirred overnight. The solvents were removed under reduce pressure and the residue was dissolved in dichloromethane and washed twice with water. The organic phase was dried over anhydrous sodium sulfate and concentrated in vacuo and the residue was purified by flash chromatography (dichloromethane/methanol: 95:5) to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08765972B2
Source datasetuspto-grants-2014_07
ORD IDord-6c6c239049f84f1c9b735809ad074a45
Source noteuspto-grants-2014_07