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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2352488Generated: November 2, 2026

Methyl iodide → HCID 23044936, compound

https://huagongshe.com/reaction/2352488

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
Reactant4-amino-N-(1-azabicyclo[2.2.2]octan-3-yl)-5-chloro-2-(cyclopropylmethoxy)benzamideHCID 71342—
SolventAcetoneHCID 180—
ProductHCID 23044936HCID 2304493679.3%

Reaction Steps

To a solution of N-(1-azabicyclo[2.2.2]oct-3-yl)-2-cyclopropylmethoxy-4-amino-5-chlorobenzamide (3.5 g; 0.01 mol) in acetone (200 ml), iodomethane (2.8 g; 0.02 moles) was added and the resulting mixture stirred to room temperature for 20 hours. The precipitated solid was collected, washed with acetone and dried to give N-(1-azabicyclo[2.2.2]oct-3-yl)-2-cyclopropylmethoxy-4-amino-5-chlorobenzamide methyl iodide (3.9 g), m.p. 274°-276° C. (d) (after recrystallisation from a mixture of acetonitrile and water).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04877780
Source datasetuspto-grants-1989_10
ORD IDord-7bc46e0e7adf44d4a0bf98f645c61ae5
Source noteuspto-grants-1989_10