HuagongsheHuagongshe Chemistry Print Report · For research reference only
Imidazole → 3-{[(Tert-butyldimethylsilyl)oxy]methyl}pyridin-2-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Imidazole | HCID 795 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | tert-Butyldimethylsilyl chloride | HCID 28928 | — |
| Reactant | (2-Aminopyridin-3-yl)methanol | HCID 11159325 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-{[(Tert-butyldimethylsilyl)oxy]methyl}pyridin-2-amine | HCID 18995804 | 93.1% |
Reaction Steps
To a solution of 6.2 parts of 2-amino-3-pyridinemethanol in 23.5 parts of N,N-dimethylformamide there were added 6.8 parts of 1H-imidazole and 7.5 parts of chlorodimethyl(1,1-dimethylethyl)silane. The whole was cooled for 10 min in an ice-bath and was stirred overnight at room temperature. The reaction mixture was diluted with 100 parts of water and the product was extracted with 1,1'-oxybisethane (2x). The combined extracts were washed with water and NaCl (sat.), dried, filtered and evaporated, yielding 11.1 parts (93.1% ) of 3-[[dimethyl(1,1-dimethylethyl)silyloxy]methyl]-2-pyridinamine (interm. 1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05482943 |
| Source dataset | uspto-grants-1996_01 |
| ORD ID | ord-f3f70cfd08544cc6997f4a9264eb51db |
| Source note | uspto-grants-1996_01 |