Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 82759Generated: October 25, 2026

(1-methyl-1H-imidazol-2-yl)methanol → HCID 178480589, compound

https://huagongshe.com/reaction/82759

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(1-methyl-1H-imidazol-2-yl)methanolHCID 573612—
ReactantKOtBu THFHCID 66863523—
ReactantHCID 178441320HCID 178441320—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178480589HCID 17848058948.9%

Reaction Steps

A solution of (1-methyl-1H-imidazol-2-yl)methanol (109 mg, 0.94 mmol) in THF (5 mL) was treated with a 1 M KOtBu/THF (0.95 mL, 0.944 mmol) and stirred for 15 min. A solution of Example 1A (190 mg, 0.47 mmol) was added to the reaction mixture and stirred for 6 hours. The reaction mixture was quenched with saturated NH4Cl solution, concentrated in vacuo and partitioned between EtOAc and brine, dried (MgSO4), filtered, and concentrated. The residue was purified by using an Analogix® Intelliflash280™ (SiO2, 0-60% ethyl acetate in hexanes) to afford the title compound (120 mg, 33% yield). 1H NMR (300 MHz, DMSO-d6) δ ppm 1.31 (s, 9 H), 1.50-1.66 (m, 1 H), 1.68-1.96 (m, 3 H), 3.55-3.84 (m, 5 H), 4.05-4.32 (m, 3 H), 5.29 (s, 2 H), 6.86 (s, 1 H), 7.20 (s, 1 H), 7.26 (s, 1 H), 7.52 (d, J=8.8 Hz, 1 H), 7.79 (dd, J=9.0, 2.2 Hz, 1 H), 8.01 (d, J=2.4 Hz, 1 H). MS (DCI/NH3) m/z 523 (M+H)+. Anal. calcd for C25H29F3N4O3S: C, 57.46; H, 5.59; N, 10.72. Found: C, 56.96; H, 5.57; N, 10.46.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846730B2
Source datasetuspto-grants-2014_09
ORD IDord-ce5a40eec2ad49d188b91777bcbdb2af
Source noteuspto-grants-2014_09