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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1595409Generated: November 1, 2026

Methanol → HCID 178440775, compound

https://huagongshe.com/reaction/1595409

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantGlutaraldehydeHCID 3485—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 178440776HCID 178440776—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178440775HCID 17844077510.3%

Reaction Steps

5-(4-Aminophenyl)-2-(4-tert-butylphenyl)-N-(2-thiazolyl)-imidazole-4-carboxamide (1.0 g) obtained in Example 77 was dissolved in tetrahydrofuran (55 ml), methanol (55 ml) and KH2PO4-Na2HPO4 buffer (pH 6.5, 70 ml), and 25% glutaraldehyde aqueous solution (1.22 g) and sodium cyanoborohydride (1.32 g) were added under ice-cooling. The mixture was stirred at room temperature for 17 days. Water (100 ml) was added and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated aqueous hydrogencarbonate solution and saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure and the residue was subjected to silica gel column chromatography to give the objective 2-(4-tert-butylphenyl)-5-(4-piperidinophenyl)-N-(2-thiazolyl)-imidazole-4-carboxamide (0.12 g), melting point 250-252° C. (decomposition).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06288061B1
Source datasetuspto-grants-2001_09
ORD IDord-57678c6144894d259342a6384d952d80
Source noteuspto-grants-2001_09