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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1903643Generated: October 30, 2026

Pipecolic Acid → 2-(4-chloro-2-fluoro-5-isopropoxyphenyl)-5,6,7,8-tetrahydroimidazo[1,5-a]pyridine-1,3(2H,8aH)-dione

https://huagongshe.com/reaction/1903643

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPipecolic AcidHCID 849—
ReactantSodium HydroxideHCID 14798—
Reactant4-Chloro-2-fluoro-5-isopropoxyphenyl isocyanateHCID 13272924—
SolventChlorobenzeneHCID 7964—
Product2-(4-chloro-2-fluoro-5-isopropoxyphenyl)-5,6,7,8-tetrahydroimidazo[1,5-a]pyridine-1,3(2H,8aH)-dioneHCID 1328121517.6%

Reaction Conditions

Temperature20 °C

Reaction Steps

A solution of 4-chloro-2-fluoro-5-isopropoxyphenyl isocyanate (2.3 g) in chlorobenzene (10 ml) was added to a 2% aqueous solution of sodium hydroxide (25 ml) containing pipecolic acid (1.3 g), and the mixture was stirred at room temperature (ca. 20° C.) for 3 hours. After allowed to stand overnight, the precipitated crystals were collected by filtration and washed with ether. The crystals were combined with water (20 ml) and adjusted to pH 2 or less with hydrochloric acid, followed by reflux for 3 hours. After allowed to cool, the mixture was extracted with ether, dried and concentrated. The residue was purified by silica gel chromatography to give 0.6 g of 2-(4-chloro-2-fluoro-5-isopropoxyphenyl)-5,6,7,8-tetrahydroimidazo[1,5-a]pyridine-1,3(2H,8aH)-dione (Compound No. 7). M.P. 60.5°-64.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04437877
Source datasetuspto-grants-1984_03
ORD IDord-606e09dbdb0841469e61d485e6867324
Source noteuspto-grants-1984_03