HuagongsheHuagongshe Chemistry Print Report · For research reference only
Imidazole → 6-Bromo-2-((tert-butyldimethylsilyloxy)methyl)imidazo[1,2-a]pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Imidazole | HCID 795 | — |
| Reactant | tert-Butyldimethylsilyl chloride | HCID 28928 | — |
| Reactant | (6-Bromoimidazo[1,2-a]pyridin-2-yl)methanol | HCID 15098897 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 6-Bromo-2-((tert-butyldimethylsilyloxy)methyl)imidazo[1,2-a]pyridine | HCID 71284789 | 69% |
Reaction Steps
To solution of (6-bromoimidazo[1,2-a]pyridin-2-yl)methanol (3.21 g, 14.13 mmol) in DCM (50 mL) was added imidazole (1.30 g, 19.09 mmol) followed by TBSCl (2.60 g, 17.25 mmol). Reaction mixture was stirred at room temperature for 30 min then was diluted with DCM (50 mL) and washed with H2O (50 mL). Organic phase was washed with NaCl (aqueous saturated, 50 mL) and dried over Na2SO4. Solvent was concentrated and residue purified by column chromatography using EtOAc/hexanes (gradient 0-50%) to afford 6-bromo-2-((tert-butyldimethylsilyloxy)methyl)imidazo[1,2-a]pyridine (3.32 g) in 69% yield as pale yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09409905B2 |
| Source dataset | uspto-grants-2016_08 |
| ORD ID | ord-0aee9ea0144641f7addfc5121ad05b2a |
| Source note | uspto-grants-2016_08 |