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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1934656Generated: October 30, 2026

Formaldehyde → HCID 22467612, compound

https://huagongshe.com/reaction/1934656

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 22467525HCID 22467525—
CatalystAcetic AcidHCID 176—
SolventMethanolHCID 887—
ProductHCID 22467612HCID 2246761278.5%

Reaction Steps

To a mixture of 5-nitro-2-(4-piperidinylamino)-N-(1,3-benzodioxol-5-ylmethyl)benzamide (80.0 mg) and 37% formaldehyde solution (192 mg) in methanol (4 mL) were added sodium cyanoborohydride (37.9 mg) and acetic acid (4 drops). After stirring for 2 hours at ambient temperature, the mixture was partitioned between an aqueous saturated sodium bicarbonate solution and chloroform. The organic layer was separated and washed with water and brine. Then, the resultant was dried over magnesium sulfate and evaporated in vacuo. The residue was triturated with diisopropyl ether to give 2-(1-methyl-4-piperidinylamino)-5-nitro-N-(1,3-benzodioxol-5-ylmethyl)benzamide as yellow powders (65.0 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06384080B1
Source datasetuspto-grants-2002_05
ORD IDord-761ca8837faa42dfa86897dc5e46a6a1
Source noteuspto-grants-2002_05