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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2055544Generated: November 1, 2026

Formaldehyde → HCID 59657570, compound

https://huagongshe.com/reaction/2055544

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantTriethylamineHCID 8471—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 69014875HCID 69014875—
SolventMethanolHCID 887—
ProductHCID 59657570HCID 5965757076%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 0.050 g (0.12 mmol) 1′-(1,2,3,4-tetrahydropyrazino[1,2-a]indol-10-ylcarbonyl)-3H-spiro[2-benzofuran-1,4′-piperidine]hydrochloride, 0.033 ml (0.24 mmol) triethylamine and 0.028 g (0.94 mmol) paraformaldehyde in 2 ml methanol was heated at reflux for 1 h. The reaction mixture was cooled to 0° C. on an ice-water bath and treated with 0.011 g (0.18 mmol) sodium cyanoborohydride. After completed addition the mixture was allowed to warm to room temperature and stirred for 2 h. Quenching with water and dilution with 2 M aqueous sodium carbonate solution was followed by extraction with dichloromethane (2×50 ml). The combined organic layers were dried over sodium sulfate, concentrated in vacuo and purified by flash-chromatography (aminopropyl-modified silica gel, n-heptane/ethyl acetate) to give the title compound (0.036 g, 76%) as an off-white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07332501B2
Source datasetuspto-grants-2008_02
ORD IDord-1b94387c9c264b449f1351f62b6ad2f8
Source noteuspto-grants-2008_02