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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1383471Generated: October 30, 2026

3-Cyclopentyloxy-4-methoxybenzamide → Piclamilast

https://huagongshe.com/reaction/1383471

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Cyclopentyloxy-4-methoxybenzamideHCID 2779330—
Reactant3,4,5-TrichloropyridineHCID 3786531—
ReactantPotassium tert-butoxideHCID 23665647—
SolventTolueneHCID 1140—
ProductPiclamilastHCID 154575—

Reaction Steps

Alternatively, a suspension of 3-cyclopentyloxy-4-methoxybenzamide (2.58 g; that is prepared as described in Reference Example 73) in dry toluene (40 mL) is heated at reflux and treated with potassium t-butoxide (1.4 g), followed by 3,4,5-trichloro-pyridine (1.82 g). The mixture is then heated at reflux for 3 hours and 45 minutes, and is then treated with a further quantity of potassium t-butoxide (1.4 g) and heated at reflux for a further period of 7 hours. The mixture is allowed to cool and is then filtered. The filtrate is evaporated and the resulting residue is extracted with aqueous sodium hydroxide solution (2 M). The alkaline solution is then acidified by treatment with acetic acid, and the solid which separates is collected by filtration, washed with water and dried, to give N-(3,5-dichloropyrid-4-yl)-3-cyclopentyloxy-4-methoxy-benzamide (2.09 g) in the form of a buff solid, m.p. 153-155° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06255326B1
Source datasetuspto-grants-2001_07
ORD IDord-e6fa6abd157d4dfdbef92313c6835728
Source noteuspto-grants-2001_07