HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 8-Benzyloxy-3-dimethylaminoethyl-2-methyl-5,6,7,8-tetrahydroimidazo[1,2-a]pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Dimethylamine, hydrochloride | HCID 10473 | — |
| Reactant | 8-Benzyloxy-2-methyl-5,6,7,8-tetrahydroimidazo[1,2-a]pyridine | HCID 13900339 | — |
| Product | 8-Benzyloxy-3-dimethylaminoethyl-2-methyl-5,6,7,8-tetrahydroimidazo[1,2-a]pyridine | HCID 54431096 | — |
Reaction Steps
A mixture consisting of the product of Example 20 (1.52 g), dimethylamine hydrochloride (565 mg), paraformaldehyde (238 mg) and ethanol (10 ml) was refluxed for four hrs. After cooling to room temperature, the solvent was evaporated under reduced pressure. The residue was dissolved in chloroform, the solution washed four times with 5% aqueous potassium carbonate, dried over Na2SO4 and then the solvent was evaporated on a rotary evaporator. The residue was chromatographed on silica gel, eluting with acetone, to obtain the title compound (m.p. 68°-70° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04450164 |
| Source dataset | uspto-grants-1984_05 |
| ORD ID | ord-021ba16a21634f3dbd1cb3d6908f5b92 |
| Source note | uspto-grants-1984_05 |