Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 349271Generated: October 26, 2026

Ammonium Chloride → 1-(3,5-Bis-trifluoromethyl-benzyl)-5-pyridin-3-yl-1H-imidazole-4-carboxylic acid methoxy-N-methyl-amide

https://huagongshe.com/reaction/349271

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantMethanamine, N-methoxy-, hydrochloride (1:1)HCID 81138—
Reactant1-(3,5-Bis-trifluoromethyl-benzyl)-5-pyridin-3-yl-1H-imidazole-4-carboxylic acid methyl esterHCID 86601224—
ReactantHCID 178418918HCID 178418918—
SolventTetrahydrofuranHCID 8028—
Product1-(3,5-Bis-trifluoromethyl-benzyl)-5-pyridin-3-yl-1H-imidazole-4-carboxylic acid methoxy-N-methyl-amideHCID 86601223—

Reaction Conditions

Temperature0 °C

Reaction Steps

Combine 1-(3,5-Bis-trifluoromethyl-benzyl)-5-pyridin-3-yl-1H-imidazole-4-carboxylic acid methyl ester (0.46 g, 1.1 mmol) and N,O-dimethyl-hydroxylamine-HCl (0.16 g, 1.6 mmol) in THF (5.5 mL). Chill to 0° C., then slowly add isopropyl magnesium chloride (2M/THF, 1.6 mL, 3.2 mmol). After 45 min., warm to RT. Add 70% sat. aq. NH4Cl, and extract with EtOAc. Dry over MgSO4, filter, and concentrate. Purify by flash chromatography on silica gel to give the title compound: MS (ES) 459.2 (M+1); 1H NMR (300 MHz, CDCl3) δ 8.63 (d, J=4.8 Hz, 1H), 8.52 (app d, 1H), 7.79 (s, 1H), 7.73 (s, 1H), 7.63 (app d, J=8.1 Hz, 1H), 7.35–7.31 (m, 1H), 7.30 (s, 2H), 5.21 (s, 2H), 3.79 (s, 3H), 3.37 (br s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07179804B2
Source datasetuspto-grants-2007_02
ORD IDord-1d620498278a43cfb22537f8241c13f0
Source noteuspto-grants-2007_02