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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1253682Generated: November 2, 2026

Acetyl chloride → HCID 67546846, compound

https://huagongshe.com/reaction/1253682

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
ReactantHCID 66701191HCID 66701191—
SolventEthanolHCID 702—
ProductHCID 67546846HCID 67546846—

Reaction Steps

The synthesis was carried out analogously to the synthesis of amine AMN-07. For this, in step (i) tert-butyl 2,7-diazaspiro[4.5]decane-7-carboxylate was reacted with 4-chloropyridinium chloride (yield: 41%). The Boc protective group was then split off. In step (ii), ethanol (6 ml) and acetyl chloride (0.27 ml, 3.94 mmol) were added to tert-butyl 2-(pyridin-4-yl)-2,7-diazaspiro[4.5]decane-7-carboxylate (0.25 g, 0.788 mmol) and the mixture was stirred at room temperature for 12 h. When the reaction was complete, the solvent was removed in vacuo. Yield: 0.23 g (89%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08455475B2
Source datasetuspto-grants-2013_06
ORD IDord-1f1ca354bd1142959cc6b130d589fbf0
Source noteuspto-grants-2013_06