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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1767781Generated: November 2, 2026

Tetrahydrofuran → HCID 178497004, compound

https://huagongshe.com/reaction/1767781

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantN-bromobutanimideHCID 67184—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
ReactantHCID 178497005HCID 178497005—
SolventMethanolHCID 887—
SolventMeOH tetrahydrofuranHCID 21899815—
ProductHCID 178497004HCID 17849700479.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

7-Fluoro-6-o-tolylamino-1H-benzoimidazole-5-carboxylic acid methyl ester 7a (2.00 g, 6.68 mmol) is suspended in 1:1 THF:MeOH mixture (60 mL) and cooled to −78° C. under a nitrogen atmosphere. A solution of NBS (1.20 g, 6.75 mmol) in 1:1 THF/MeOH (5 mL) is added followed by a MeOH (5 mL) solution of TsOH.H2O (1.9 g, 10.0 mmol). After 30 minutes, the reaction mixture is warmed to 0° C. and then after 1 hour warmed to rt. After 16 hours, more NBS (0.12 g, 0.67 mmol) is added and the reaction mixture is allowed to stir for 3 hours. The reaction mixture is quenched by the addition of 10% Na2S2O4 solution. After 30 minutes, the reaction mixture is diluted with water and ethyl acetate and the layers separated. The aqueous layer is extracted with ethyl acetate. The combined organic extracts are dried (Na2SO4) and concentrated under reduced pressure. The recovered solid is triturated with methylene chloride to give 2.00 g (79%) pure desired product: MS APCI (+) m/z 380, 378 (M+1 Br pattern) detected.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07235537B2
Source datasetuspto-grants-2007_06
ORD IDord-0093bcbd07074506ad324c50acb42873
Source noteuspto-grants-2007_06