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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1253681Generated: November 4, 2026

Acetyl chloride → HCID 67546430, compound

https://huagongshe.com/reaction/1253681

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
ReactantHCID 66700746HCID 66700746—
SolventEthanolHCID 702—
ProductHCID 67546430HCID 67546430—

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-2-carboxylate was reacted with 4-chloropyridinium chloride (yield: 53%). The Boc protective group was then split off. In step (ii), ethanol (8 ml) and acetyl chloride (0.37 ml, 5.355 mmol) were added to tert-butyl 7-(pyridin-4-yl)-2,7-diazaspiro[4.5]decane-2-carboxylate (0.34 g, 1.071 mmol) and the mixture was stirred at room temperature for 12 h. When the reaction was complete, the solvent was removed in vacuo. Yield: 0.28 g (80%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08455475B2
Source datasetuspto-grants-2013_06
ORD IDord-0c603b5728f5436bac692a7239adc74a
Source noteuspto-grants-2013_06