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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 719610Generated: October 30, 2026

Sodium borohydride → HCID 178513580, compound

https://huagongshe.com/reaction/719610

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 178513579HCID 178513579—
SolventMethanolHCID 887—
ProductHCID 178513580HCID 17851358087.4%

Reaction Steps

To a solution of 2-(4-benzoyl-phenyl)-1H-benzoimidazole-5-carboxylic acid amide (Example 3,18 mg, 0.05 mmol) in anhydrous methanol (2.0 mL) was added sodium borohydride (2.0 mg, 0.05 mmol) in one portion. The reaction mixture was stirred under N2 for 1 h. The solvent was removed under reduced pressure, and the residue was re-dissolved in 1:1 ethyl acetate/H2O (40 mL). The solution was washed with H2O (20 mL) then brine (20 mL) and dried (Na2SO4). Solvent was removed under reduced pressure, and purification by chromatography (silica gel, 1% methanol saturated with ammonia/9% methanol/CH2Cl2) afforded 15 mg (83%) of the title compound. TLC (silica, 1% methanol saturated with ammonia/9% methanol/CH2Cl2): Rf=0.13. HPLC (Method A): Rt=6.36. MS (ESI+): mass calculated for C21H17N3O2, 343.1; m/z found, 344.1 [M+H]+. 1H NMR (400 MHz, CD3OD): δ 8.17 (br s, 1H), 8.07 (d, J=8.4 Hz, 2H), 7.82–7.80 (dd, J=8.4, 1.4 Hz, 1H), 7.63 (br d, J=6.7 Hz, 1H), 7.58 (d, J=8.2 Hz, 2H), 7.42–7.40 (dd, J=8.5, 1.4 Hz, 2H), 7.32 (t, J=7.5 Hz, 2H), 7.26–7.22 (m, 1H), 5.85 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07132440B2
Source datasetuspto-grants-2006_11
ORD IDord-ecc20c10a71a4dd0882ee3ff5c760aea
Source noteuspto-grants-2006_11