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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2250392Generated: November 1, 2026

Sodium hydride → HCID 178474147, compound

https://huagongshe.com/reaction/2250392

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantN-(6-Formyl-4-methylpyridin-2-YL)acetamideHCID 72214398—
ReactantHCID 178454879HCID 178454879—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178474147HCID 178474147—

Reaction Conditions

Temperature90 °C

Reaction Steps

5.0 g of 6-brom-3H-midazo[4,5-b]pyridin-2-yl-methyl-tributyl-phosphonium-chloride (compound A5) are suspended in 50 ml of tetrahydrofuran and added to a suspension of sodium hydride (60% strength) in 50 ml tetrahydrofuran at room temperature. After vigorously stirring for 10 min, 1.43 g of N-(6-formyl-4-methyl-pyridin-2-yl)-acetamide (compound B11) is added in portions (10 min). Subsequently, the suspension is heated at 90° C. for 22 h. Thereafter, the mixture is filtered with suction and the remaining residue is rinsed with tetrahydrofuran. The pure title compound is obtained by evaporating the filtrate to dryness to afford 1.88 g of an amorphous solid. M.p. >350° C. ESI-MS: 372.1/374.1 (MH+; 99%/100%). TLC: Rf=0.50 (dichloromethane/methanol 10:1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07317021B2
Source datasetuspto-grants-2008_01
ORD IDord-cd51aa7d6326442991b8f198107c9256
Source noteuspto-grants-2008_01