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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2076406Generated: November 1, 2026

Formaldehyde → 7-(5-Ethoxypyridin-3-yl)-1-methyl-1,7-diazaspiro[4.4]nonane

https://huagongshe.com/reaction/2076406

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantSodium BicarbonateHCID 516892—
Reactant7-(5-Ethoxypyridin-3-yl)-1,7-diazaspiro[4.4]nonaneHCID 22291242—
SolventFormic AcidHCID 284—
Product7-(5-Ethoxypyridin-3-yl)-1-methyl-1,7-diazaspiro[4.4]nonaneHCID 2229121889.3%

Reaction Steps

To a stirring solution of 7-(5-ethoxy-3-pyridyl)-1,7-diazaspiro[4.4]nonane (360.4 mg, 1.4 mmol) in 37% aqueous solution of formaldehyde (4 mL) was added 98% formic acid (2 mL) under nitrogen. The reaction mixture was heated to reflux for 8 h. The reaction mixture was cooled to room temperature, then basified with saturated aqueous sodium bicarbonate to pH 8-9 and extracted with chloroform (4×15 mL). The combined chloroform extracts were dried (Na2SO4), filtered and concentrated by rotary evaporation to afford a viscous brown liquid. This was distilled using a Kugelrohr apparatus (2 mm, 180° C.) to give a very light cream-colored syrup (340 mg, 89.3%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07923559B2
Source datasetuspto-grants-2011_04
ORD IDord-645a7cac09414a5398f9ff6f58c495bf
Source noteuspto-grants-2011_04