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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 912947Generated: October 30, 2026

HCID 178461548, compound → HCID 178461544, compound

https://huagongshe.com/reaction/912947

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 178461548HCID 178461548—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
SolventSodium HydroxideHCID 14798—
ProductHCID 178461544HCID 178461544—

Reaction Steps

To a solution of N-{2-[(2R)-4-(3-chloro-5-hydroxymethyl-pyridin-2-yl)-2-methyl-piperazin-1-yl]-6-trifluoromethyl-3H-benzoimidazol-4-yl}-3,4,5-trifluoro-benzamide (120 mg, 0.2 mmol, Example 170c) in THF (1 mL) was added BH3. THF (0.6 mL, 0.6 mmol, Aldrich) dropwise with stirring at 0° C. The mixture was heated at reflux for 5 h, cooled to room temperature and diluted with 1:1 mixture of MeOH and 1N NaOH (2 mL). The mixture was stirred at room temperature for 30 min and extracted with EtOAc (2×20 mL). The combined organic extracts were washed with brine (10 mL), dried over Na2SO4 and filtered. The filtrate was evaporated in vacuo and the residue was purified by silica gel column chromatography, eluting with 5% MeOH/CH2Cl2 to give the title compound as a white solid. MS (ESI, pos. ion) m/e: 586 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08026241B2
Source datasetuspto-grants-2011_09
ORD IDord-45ddf459486c4515a06459549b4f787a
Source noteuspto-grants-2011_09