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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1254684Generated: November 2, 2026

Imidazole → HCID 67006584, compound

https://huagongshe.com/reaction/1254684

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
ReactantHCID 67006661HCID 67006661—
SolventDimethylformamideHCID 6228—
ProductHCID 67006584HCID 6700658465.3%

Reaction Conditions

Temperature0 °C

Reaction Steps

The crude material 4-cyano-N′-((2R,3R)-2-(4-cyano-2-methyl-3-(trifluoromethyl)phenylamino)-3-hydroxybutanoyl)benzohydrazide (800 mg, 1.75 mmol) was added to DMF (40 mL), followed by addition of TBDMS-Cl (1.06 g, 7.00 mmol) and imidazole (954 mg, 14.01 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 extract with EtOAc. The resulting crude material was chromatographed to get the desired product (640 mg) 1H NMR (400 MHz, acetone-d6, δ in ppm): 9.62 (br s), 7.93 (d, J=9 Hz, 2H), 7.79 (d, J=9 Hz, 2H), 7.55 (d, J=9 Hz, 1H), 6.98 (d, J=9 Hz, 1H), 5.38 (d, J=9 Hz, 1H), 4.41 (m, 1H), 4.18 (m, 1H), 2.25 (m, 3H), 1.31 (d, J=6 Hz, 3H), 0.77 (s, 9H), 0.03 (s, 6H), 0.00 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08455525B2
Source datasetuspto-grants-2013_06
ORD IDord-fc59ec0191964c169760aa11fe318e72
Source noteuspto-grants-2013_06