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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1182736Generated: October 30, 2026

Formaldehyde → HCID 46213853, compound

https://huagongshe.com/reaction/1182736

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 67378312HCID 67378312—
SolventMethanolHCID 887—
ProductHCID 46213853HCID 46213853—

Reaction Steps

A mixture of the crude 1′-(8-chloro-5,6-dihydro-4H-[1,2,4]triazolo[4,3-a][1,4]benzodiazepin-1-yl)-1H-spiro[isochromene-4,4′-piperidine] (0.10 g, 0.24 mmol) and paraformaldehyde (0.057 g, 1.9 mmol) in methanol (2 ml) was heated at reflux for 4 h. After cooling to room temperature sodium cyanoborohydride (0.03 g, 0.47 mmol) was added at 0° C. The reaction mixture was allowed to warm to room temperature and stirred for 18 h. Quenching with 1 M aqueous sodium hydroxide solution (30 ml) was followed by extraction with ethyl acetate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08664216B2
Source datasetuspto-grants-2014_03
ORD IDord-34038a108af94c6ca96e3f86d1140ccc
Source noteuspto-grants-2014_03