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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1378695Generated: November 3, 2026

Formaldehyde → HCID 54167440, compound

https://huagongshe.com/reaction/1378695

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantAcetonitrileHCID 6342—
ReactantHCID 20726135HCID 20726135—
ReactantCID 101953985HCID 101953985—
SolventMethanolHCID 887—
ProductHCID 54167440HCID 5416744087.4%

Reaction Steps

Formaldehyde (37% aq. sol., 0.4 ml) and sodium cyanoboron hydride (138 mg) were successively added to an acetonitrile suspension (3 ml) of 400 mg of the (S)-N-{3-[3-fluoro-4-(4-methylamino-piperidin-1-yl)-phenyl]-2-oxo-oxazolidin-5-ylmethyl}-acetamide (Compound No. 70) which was synthesized in Example 18, and the mixture was stirred at room temperature for 48 h. Methanol was added and the mixture was stirred for 10 min. Thereafter, alumina (5 g) was added and the residue was evaporated under vacuum. The residue was purified by alumina column chromatography (solvent: chloroform/methanol=100/1) to afford the title compound (363 mg) in a yield of 87%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05668286
Source datasetuspto-grants-1997_09
ORD IDord-a09e035700084084a6939816d4c835c7
Source noteuspto-grants-1997_09