HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → 4-(Imidazo[1,2-a]pyridin-3-yl)piperidin-4-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | HCID 69456650 | HCID 69456650 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-(Imidazo[1,2-a]pyridin-3-yl)piperidin-4-ol | HCID 23614453 | — |
Reaction Steps
To a stirred solution of 4-hydroxy-4-imidazo[1,2-a]pyridin-3-yl-piperidine-1-carboxylic acid tert-butyl ester (2.0 g 6.26 mmol) in CH2Cl2 (100 ml) trifluoro acetic acid (10 ml) was added at room temperature. The reaction mixture was stirred at room temperature for 24 hrs. At the end, the reaction mixture was basified with methanolic ammonia and concentrated to dryness. The residue was directly chromatographed over silica-gel column and eluted with methanol:10% methanolic ammonia. The product, 4-imidazo[1,2-a]pyridin-3-yl-piperidin-4-ol was obtained as yellow oil; Yield; 620 mg (48%); 218 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07235569B2 |
| Source dataset | uspto-grants-2007_06 |
| ORD ID | ord-3a5b1d94642e402d8a067c1d4b7dd0fe |
| Source note | uspto-grants-2007_06 |