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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1254704Generated: November 2, 2026

Imidazole → HCID 67006538, compound

https://huagongshe.com/reaction/1254704

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
ReactantHCID 67006549HCID 67006549—
SolventDimethylformamideHCID 6228—
ProductHCID 67006538HCID 6700653861.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

The crude material 4-cyano-N′-((2R,3S)-2-(4-cyano-2-methyl-3-(trifluoromethyl)phenylamino)-3-hydroxybutanoyl)benzohydrazide (507 mg, 1.14 mmol) was added to DMF (30 mL), followed by addition of TBDMS-Cl (686 mg, 4.55 mmol) and imidazole (619 mg, 9.10 mmol) at 0° C. The solution was allowed to stir at 0° C. for 30 min and then at room temperature for overnight. The reaction was quenched with the addition of 200 mL brine and extracted with EtOAc. The resulting crude material was chromatographed to give the desired product (390 mg) 1H NMR (400 MHz, acetone-d6, δ in ppm): 9.6 (br s), 7.92 (d, J=9 Hz, 2H), 7.8 (d, J=9 Hz, 2H), 7.56 (d, J=9 Hz, 1H), 6.92 (d, J=9 Hz, 1H), 5.55 (d, J=9 Hz, 1H), 4.51 (m, 1H), 4.16 (m, 1H), 2.25 (m, 3H), 1.24 (d, J=6 Hz, 3H), 0.82 (s, 9H), 0.05 (s, 6H), 0.00 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08455525B2
Source datasetuspto-grants-2013_06
ORD IDord-1ea443c961bf4be6988963246e9d5eed
Source noteuspto-grants-2013_06