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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 374767Generated: October 31, 2026

Imidazole → 3-{[(Tert-butyldimethylsilyl)oxy]methyl}pyridin-2-amine

https://huagongshe.com/reaction/374767

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantDimethylformamideHCID 6228—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
Reactant(2-Aminopyridin-3-yl)methanolHCID 11159325—
SolventWaterHCID 962—
Product3-{[(Tert-butyldimethylsilyl)oxy]methyl}pyridin-2-amineHCID 1899580493.1%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05482943
Source datasetuspto-grants-1996_01
ORD IDord-f3f70cfd08544cc6997f4a9264eb51db
Source noteuspto-grants-1996_01