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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1295853Generated: October 30, 2026

Methanol → HCID 20780214, compound

https://huagongshe.com/reaction/1295853

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantHCID 21916126HCID 21916126—
Reactant3-(Cycloundecen-1-yl)-1,2-diazacycloundec-2-eneHCID 53630274—
ReactantHCID 178470341HCID 178470341—
SolventAcetoneHCID 180—
SolventTolueneHCID 1140—
ProductHCID 20780214HCID 20780214—

Reaction Steps

To a solution of 2-bromo-5-methyl-3H-imidazole-4-carboxylic acid ethyl ester (1.00 g, 4.291 mmol) and 2-bromo-N-(2,4,6-trimethyl-phenyl)-acetamide (1.209 g, 4.720 mmol) in a mixture of toluene (16 mL) and acetone (8 mL) was added diazabicycloundecene (0.71 mL, 4.720 mmol). The resulting solution was stirred at room temperature for 24 h. Methanol (10 mL) was added to dissolve the precipitate formed, followed by the addition of silica gel (25 g). The solvent was removed under reduced pressure to dryness and the residue was applied to a silica gel-packed column. The isolation of the product was achieved by column chromatography (hexanes-ethyl acetate 4:1 to 1:2). Yield—0.736 g (42%). 1H NMR (DMSO d-6, 500 MHz) δ 9.52 (s, 1H), 6.86 (s, 2H), 5.15 (br s, 2H), 4.25 (q, J=7.1 Hz, 2H), 2.38 (s, 3H), 2.21 (s, 3H), 2.11 (s, 6H), 1.30 (t, J=7.1 Hz, 3H); LC/MS: tR=1.46 min., MS: [M+H]=408.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07244746B2
Source datasetuspto-grants-2007_07
ORD IDord-9cc1c382b5784704a3f9d44f72f094e6
Source noteuspto-grants-2007_07