HuagongsheHuagongshe Chemistry Print Report · For research reference only
Imidazole → 5-[3-(tert-Butyldimethylsilanyloxymethyl)phenyl]pyridin-2-ylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Imidazole | HCID 795 | — |
| Reactant | [3-(6-Aminopyridin-3-yl)phenyl]methanol | HCID 44232377 | — |
| Reactant | Tert-butyldimethylsilane chloride | HCID 131722836 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-[3-(tert-Butyldimethylsilanyloxymethyl)phenyl]pyridin-2-ylamine | HCID 44232378 | 89.3% |
Reaction Steps
4.99 g of [3-(6-aminopyridin-3-yl)phenyl]methanol are placed in a round-bottomed flask and dissolved in 240 ml of tetrahydrofuran. 2.2 g of 1H-imidazole are added thereto, followed by 4.51 g of tert-butyldimethylsilane chloride, and the mixture is left to stir at ambient temperature for 48 hours. The reaction mixture is then hydrolysed with water, and the organic phase, which has been extracted with ethyl acetate, is separated, dried over magnesium sulphate and concentrated under reduced pressure. The residue obtained is purified by silica gel chromatography, elution being carried out with a heptane/ethyl acetate mixture. 7.0 g of compound are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08338451B2 |
| Source dataset | uspto-grants-2012_12 |
| ORD ID | ord-f9556880a3d8426c89bfce34dc9eb02a |
| Source note | uspto-grants-2012_12 |