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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1890292Generated: November 3, 2026

Sodium borohydride → HCID 178515761, compound

https://huagongshe.com/reaction/1890292

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 178515950HCID 178515950—
SolventEthanolHCID 702—
ProductHCID 178515761HCID 17851576166.9%

Reaction Steps

2-(5-Hydroxy-3H-imidazo[4,5-b]pyridin-3-yl)cyclohexanone (0.200 g, 0.865 mmol) was taken up in ethanol (4 mL) and sodium borohydride (9.8 mg, 0.26 mmol) added. The reaction was stirred at room temperature overnight. The solvent was removed under reduced pressure. The residue was purified by preparative HPLC to give the title compound (0.135 g). LCMS m/z=234.2 [M+H]+; 1H NMR (400 MHz, DMSO-d6) δ ppm 1.35-1.60 (m, 4H), 1.75-1.95 (m, 2H), 2.00-2.15 (m, 2H), 4.00-4.10 (m, 1H), 4.38 (q, J=8.1 Hz, 1H), 6.92 (d, J=8.8 Hz, 1H), 8.18 (d, J=8.8 Hz, 1H), 9.52 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08507473B2
Source datasetuspto-grants-2013_08
ORD IDord-f96e07bb732943948c038a098cbd7a91
Source noteuspto-grants-2013_08