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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1684948Generated: November 2, 2026

Imidazole → 5-(((tert-Butyldimethylsilyl)oxy)methyl)thiazol-2-amine

https://huagongshe.com/reaction/1684948

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
Reactant(2-Aminothiazol-5-yl)methanolHCID 11217273—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventDimethylformamideHCID 6228—
Product5-(((tert-Butyldimethylsilyl)oxy)methyl)thiazol-2-amineHCID 5754132844.4%

Reaction Steps

A solution of 5-(hydroxymethyl)-thiazol-2-ylamine (0.787 g, 6.05 mmol), TBDMSCl (1.003 g, 6.65 mmol) and imidazole (0.49 g, 7.26 mmol) in DMF (15 mL) is stirred at room temperature for 24 h. The reaction mixture is diluted with ether and water. The organic layer is washed with water (3×). The aqueous washings are backwashed with ether (2×). The organic layers are combined, dried over MgSO4 and condensed. The crude material is purified using a plug of silica and eluting with 1:1 petrol:ethyl acetate to give the product (0.656 g, 44%). 1H-NMR (400 MHz, d6-DMSO) =0.01 (s, 6H, 2×CH3), 0.82 (s, 9H, tBu), 4.61 (s, 2H, CH2), 4.74 (brs, 2H, NH2), 6.8 (s, 1H, CH). LCMS: Rt 2.62 min (92.7%). MS (MH+, m/z) 245.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08148369B2
Source datasetuspto-grants-2012_04
ORD IDord-8db3fd174cdd473293284a4cf0703c98
Source noteuspto-grants-2012_04