Imidazole → 5-Bromo-2-((triisopropylsilyloxy)methyl)thiazole

HRID 525528Notes

Reaction equation

HRID 525528 reaction equation
[Br:1][C:2]1[S:6][C:5]([CH2:7][OH:8])=[N:4][CH:3]=1.N1C=CN=C1.CN(C)C=O.Cl[Si:20]([CH:27]([CH3:29])[CH3:28])([CH:24]([CH3:26])[CH3:25])[CH:21]([CH3:23])[CH3:22]>C(OC(=O)C)C>[Br:1][C:2]1[S:6][C:5]([CH2:7][O:8][Si:20]([CH:27]([CH3:29])[CH3:28])([CH:24]([CH3:26])[CH3:25])[CH:21]([CH3:23])[CH3:22])=[N:4][CH:3]=1

Participants

6

Reactant 4

HCID 795ImidazoleHCID 6228DimethylformamideHCID 139400Triisopropylsilyl chlorideHCID 11953783(5-Bromo-1,3-thiazol-2-yl)methanol

Product 1

HCID 866954185-Bromo-2-((triisopropylsilyloxy)methyl)thiazoleYield 104%

Reagents, catalysts & solvents 1

HCID 8857Ethyl AcetateSolvent

Procedure

A 100 mL round bottom flask is charged with (5-bromothiazol-2-yl)methanol (2.5 g, 12.9 mmol), imidazole (1.75 g, 25.8 mmol), dimethylformamide (25 mL), and chlorotriisopropylsilane (3.4 mL, 15.5 mmol). The reaction is stirred at room temperature under nitrogen for 72 hours. Contents are diluted with ethylacetate (150 mL), washed with 0.5M hydrochloric acid (2×100 mL) and brine (100 mL), dried (Na2SO4), and concentrated under vacuum to afford the title compound (4.7 g): m/z (Cl) M+H 350+352.

Workup

  1. washwashed with 0.5M hydrochloric acid (2×100 mL) and brine (100 mL)
  2. dry with materialdried (Na2SO4)
  3. concentrationconcentrated under vacuum

Sources & evidence

ORD record
ord-d2e18e2e7bbe4b16ab4610f73556121f
Source dataset
uspto-grants-2016_05
Patent number
US09340564B2

Reaction notes

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