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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 918200Generated: October 31, 2026

(1,5,6,7,8,8a-Hexahydroimidazo[1,5-a]pyridin-3-yl)(phenyl)methanone → HCID 21523494, compound

https://huagongshe.com/reaction/918200

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(1,5,6,7,8,8a-Hexahydroimidazo[1,5-a]pyridin-3-yl)(phenyl)methanoneHCID 71398802—
ReactantHCID 178424303HCID 178424303—
ReactantHCID 178491912HCID 178491912—
ProductHCID 21523494HCID 21523494—
ProductHCID 21523496HCID 21523496—

Reaction Steps

In an analogous manner, reaction of the ketone of Example 2 with m-chlorophenylmagnesium bromide and p-chlorophenylmagnesium bromide gives respectively α-(m-chlorophenyl)-α-phenyl-1,5,6,7,8,8a-hexahydroimidazo[1,5-a]pyridine-3-methanol and α-(p-chlorophenyl)-α-phenyl-1,5,6,7,8,8a-hexahydroimidazo[1,5-a]pyridine 3-methanol. Similarly, reaction of the ketone of Example 2 with p-methoxyphenylmagnesium bromide and o-methylphenylmagnesium bromide gives respectively α-(p-methoxyphenyl)-α-phenyl-1,5,6,7,8,8a-hexahydroimidazo[1,5-a]pyridine-3-methanol and α-(o-methylphenyl)-α-phenyl-1,5,6,7,8,8a-hexahydroimidazo[1,5-a]pyridine-3-methanol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03969528
Source datasetuspto-grants-1976_07
ORD IDord-9283239f68ae411b9d7bef502acae323
Source noteuspto-grants-1976_07