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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1253680Generated: November 1, 2026

Acetyl chloride → HCID 66701188, compound

https://huagongshe.com/reaction/1253680

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
ReactantHCID 66701123HCID 66701123—
SolventEthanolHCID 702—
ProductHCID 66701188HCID 66701188—

Reaction Steps

The synthesis was carried out analogously to the synthesis of amine AMN-07. For this, in step (i) tert-butyl 2,8-diazaspiro[5.5]undecane-2-carboxylate was reacted with 4-chloropyridinium chloride (yield: 66%). The Boc protective group was then split off. In step (ii), ethanol (8 ml) and acetyl chloride (0.45 ml, 6.335 mmol) were added to tert-butyl 8-(pyridin-4-yl)-2,8-diazaspiro[5.5]undecane-2-carboxylate (0.42 g, 1.267 mmol) and the mixture was stirred at room temperature for 12 h. When the reaction was complete, the solvent was removed in vacuo. Yield: 0.39 g (90%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08455475B2
Source datasetuspto-grants-2013_06
ORD IDord-5516dabc27524bc2b8e410c4c2de3b0b
Source noteuspto-grants-2013_06