HuagongsheHuagongshe Chemistry Print Report · For research reference only
(1,5,6,7,8,8a-Hexahydroimidazo[1,5-a]pyridin-3-yl)(phenyl)methanone → HCID 21523491, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (1,5,6,7,8,8a-Hexahydroimidazo[1,5-a]pyridin-3-yl)(phenyl)methanone | HCID 71398802 | — |
| Reactant | HCID 178478127 | HCID 178478127 | — |
| Reactant | HCID 178478191 | HCID 178478191 | — |
| Product | HCID 21523491 | HCID 21523491 | — |
| Product | HCID 21523495 | HCID 21523495 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03969528 |
| Source dataset | uspto-grants-1976_07 |
| ORD ID | ord-5517bc82da1147bfa0e96635de569434 |
| Source note | uspto-grants-1976_07 |