Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1594115Generated: November 4, 2026

Formamide → HCID 22379917, compound

https://huagongshe.com/reaction/1594115

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormamideHCID 713—
ReactantPhosphorus sulfide (P2S5)HCID 14817—
ReactantBromineHCID 24408—
ReactantMethanethioamideHCID 3005587—
ReactantHCID 22379891HCID 22379891—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 22379917HCID 22379917—

Reaction Steps

A mixture of 3-(5-bromo-1-ethyl-1H-benzoimidazol-2-yl)-1-(3-fluoro-phenyl)-propan-1-one (0.2 g, 0.53 mmol) and bromine (0.1 g, 0.62 mmol) is refluxed in 1,4-dioxane for 2 hours. Thioformamide (freshly made from formamide and P2S5 in 1,4-dioxane) (1.3 mmol) are added to the solution. The mixture is refluxed overnight. The solvent is removed and NaHCO3 (aq.) (15 mL) and DCM (40 mL) are added to the residue. The organic layer is separated and the aqueous layer is extracted with DCM (2×30 mL). The combined organic layers are dried and solvent removed. The crude is purified by PTLC (5% methanol in DCM) to give 5-bromo-1-ethyl-2-[4-(3-fluoro-phenyl)-thiazol-5-ylmethyl]-1H-benzoimidazole. 1H NMR (CDCl3) δ 8.78 (s, 1H), 7.91 (s, 1H), 7.38-7.48 (m, 4H), 7.11-7.19 (m, 2H), 4.59 (s, 2H), 3.90 (q, 2H), 1.12 (t, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07300945B2
Source datasetuspto-grants-2007_11
ORD IDord-22e87f330f484c42899fe63dc58e964e
Source noteuspto-grants-2007_11