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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 344507Generated: October 27, 2026

5-(Cyclohexylmethoxy)pentyl bromide → 4-amino-5-chloro-2-methoxy-N-((1-(5-(cyclohexylmethoxy)pentyl)piperidin-4-yl)methyl)benzamide hydrochloride

https://huagongshe.com/reaction/344507

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-(Cyclohexylmethoxy)pentyl bromideHCID 54015431—
Reactant4-amino-5-chloro-2-methoxy-N-(piperidin-4-ylmethyl)benzamide dihydrochlorideHCID 69966330—
Product4-amino-5-chloro-2-methoxy-N-((1-(5-(cyclohexylmethoxy)pentyl)piperidin-4-yl)methyl)benzamide hydrochlorideHCID 7007628648.8%

Reaction Steps

4-Amino-5-chloro-2-methoxy-N-(piperidin-4-ylmethyl)benzamide dihydrochloride (1.50 g) as starting compound and 5-(cyclohexylmethoxy)pentyl bromide (1.30 g) were reacted and treated in the same manner as in Example 168 to give 0.51 g of 4-amino-5-chloro-2-methoxy-N-((1-(5-(cyclohexylmethoxy)pentyl)piperidin-4-yl)methyl)benzamide hydrochloride.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05864039
Source datasetuspto-grants-1999_01
ORD IDord-a67f5f59bffe4a9cbd7adae05cce101e
Source noteuspto-grants-1999_01