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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1793743Generated: November 4, 2026

HCID 135681577, compound → HCID 135681640, compound

https://huagongshe.com/reaction/1793743

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 135681577HCID 135681577—
SolventTetrahydrofuranHCID 8028—
ProductHCID 135681640HCID 13568164060%

Reaction Steps

To a solution of (±)-2-{4-[2-(3-Chloro-phenyl)-2-hydroxyethyl amino]-2-oxo-1,2-dihydro-pyridin-3-yl}-7-methyl-3H-benzimidazole-5-carboxylic acid amide (20 mg, 0.046 mmol) in THF (1 mL) was added borane-tetrahydrofuran complex (1 M solution) (0.45 mL, 0.45 mmol). The reaction mixture was stirred at room temperature for 10 h and quenched with acetic acid (2 drops). After removal of most solvent, the residue was extracted with EtOAc, washed with brine, dried over Na2SO4. After concentration, the crude product was purified by prep. HPLC to yield the title compound (11.5 mg, 60%). 1H NMR (400 MHz, CD3OD) δ 7.53 (1H, s), 7.50 (1H, s), 7.39 (1H, d, J=7.5 Hz), 7.24–7.32 (3H, m), 7.13 (1H, s), 6.26 (1H, d, J=7.5 Hz), 4.99 (1H, dd, J=4.8, 6.8 Hz), 4.19 (2H, s), 3.72 (1H, dd, J=4.8, 13.6 Hz), 3.64 (1H, dd, J=6.8, 13.6 Hz), 2.62 (3H, s). LCMS (M+H)+ m/z 424 (t=2.10 min.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07081454B2
Source datasetuspto-grants-2006_07
ORD IDord-eb2391b5125742e28ea0f4edae1dc953
Source noteuspto-grants-2006_07