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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 216504Generated: October 25, 2026

Methanol → HCID 178497006, compound

https://huagongshe.com/reaction/216504

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantN-IodosuccinimideHCID 120273—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
ReactantHCID 178497005HCID 178497005—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178497006HCID 17849700669.3%

Reaction Conditions

Temperature0 °C

Reaction Steps

7-Fluoro-6-o-tolylamino-1H-benzoimidazole-5-carboxylic acid methyl ester 7a (1.47 g, 4.92 mmol) is suspended in 1:1 THF:MeOH mixture (44 mL) and cooled to −78° C. under a nitrogen atmosphere. A solution of NIS (1.66 g, 7.39 mmol) in THF (2 mL) is added followed by a MeOH (2 mL) solution of TsOH.H2O (1.87 g, 9.84 mmol). After 30 minutes, the reaction mixture is warmed to 0° C. and 1 mL methylene chloride is added. The reaction is slowly allowed to warm to room temperature with stirring over 16 hours. The reaction mixture is quenched by the addition of 10% Na2S2O4 solution. The reaction mixture is then 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 MeOH to give 1.45 g (69%) pure desired product: MS ESI (+) m/z 426 (M+1) detected; MS ESI (−) m/z 424 (M−1) detected.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08193229B2
Source datasetuspto-grants-2012_06
ORD IDord-12c7447ffad14fd78db9c0b9cbbedb20
Source noteuspto-grants-2012_06