Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1868338Generated: November 1, 2026

Sodium borohydride → HCID 69063770, compound

https://huagongshe.com/reaction/1868338

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 86592586HCID 86592586—
SolventMethanolHCID 887—
ProductHCID 69063770HCID 6906377064.4%

Reaction Steps

4-(2-methyl-2H-benzotriazol-5-yl)-5-(6-methyl-pyridin-2-yl)-1H-imidazole-2-carbaldehyde (20 mg, 0.063 mmol) was dissolved in 2 ml anhydrous methanol. Sodium borohydride (3 mg, 0.069 mmol) was added and the reaction stirred at room temperature for 1 hour. The reaction was quenched with water and solvent was removed by rotary evaporation. The residue was purified on Biotage Flash 12S silica gel column using chloroform/methanol gradient system (97:3 to 95:5, respectively) as eluent to afford [4-(2-methyl-2H-benzotriazol-5-yl)-5-(6-methyl-pyridin-2-yl)-1H-imidazol-2-yl]-methanol (13 mg, 64% yield) as a white solid. HPLC tR=3.18 min, LC-MS=321 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07635702B2
Source datasetuspto-grants-2009_12
ORD IDord-8f6b859f079f4e21ae438f8d08ec4e8c
Source noteuspto-grants-2009_12