Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1826115Generated: November 1, 2026

Imidazole → HCID 21034347, compound

https://huagongshe.com/reaction/1826115

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantWaterHCID 962—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
ReactantHCID 23574467HCID 23574467—
SolventDimethylformamideHCID 6228—
ProductHCID 21034347HCID 21034347—

Reaction Steps

Solid TBDMS Chloride (8.22 g, 54.44 mmol) was added in one portion to a solution of 170 (7.23 g, 24.74 mmol) and imidazole (8.42 g, 123.72 mmol) in anhydrous DMF (75 mL) and allowed to stir at room temperature for 16 h. The reaction mixture was poured into water (500 mL) and filtered to afford the crude product (171), which was purified by recrystallisation from EtOH (800 mL) as fine white needles (6.995 g, 17.21 mmol, 70%). 1HNMR (270 MHz, CDCl3) δ 10.06 (s, 1H, NH), 7.37 (S, 1H, ArH), 6.68 (s, 1H, ArH), 4.19-4.14 (m, 1H, 2), 4.06-4.01 (m, 1H, 11a), 3.90 (s, 3H, OMe), 3.88 (s, 3H, OMe), 3.69-3.63 (m, 2H, 3), 2.85-2.80 (m, 1H, 1), 2.05-2.01 (m, 1H, 1); 13C NMR (67.8 MHz, CDCl3) δ 170.4, 170.2, 165.9, 152.1, 145.8, 145.6, 131.1, 130.7, 118.1, 111.9, 104.3, 104.1, 69.2, 69.1, 56.0, 55.9, 55.7, 54.3, 54.0, 35.0, 25.8, 25.7, 25.6, 17.9, −3.0, −3.5, −4.9, −5.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07049311B1
Source datasetuspto-grants-2006_05
ORD IDord-f81d69043ecf4c1793b694438859a696
Source noteuspto-grants-2006_05