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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1004593Generated: October 26, 2026

Sodium Hydroxide → HCID 15454675, compound

https://huagongshe.com/reaction/1004593

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantPotassium BromideHCID 253877—
Reactant2-(Chloromethyl)-3-methylpyridine hydrochlorideHCID 13058683—
ReactantHCID 178505405HCID 178505405—
SolventEthanolHCID 702—
ProductHCID 15454675HCID 15454675154.4%

Reaction Steps

The title compound (0.95 g, 63%) was prepared by the general procedure using, 6-fluoro-5-(piperidin-1-yl)-2-mercapto-1H-benzimidazole (0.70 g, 2.8 mmol) (obtained in preparation 3), 4-(piperidin-1-yl)-3 )-methyl-2-chloromethylpyridine hydrochloride (0.91 g, 3.5 mmol), sodium hydroxide (0.30 g, , 7.7 mmol) and ethanol (15 mL). mp 161-162° C.; IR (KBr) 3430, 1581, 1429 cm-1 ; 1H NMR (CDCl3) δ 1.60 (m, 4H, 2×CH2), 1.74 (m, 8H, 2×(CH2)2), 2.30 (s, 3)H, CH3), 3.00 (m, 8H, 2×N(CH2)2), 4.32 (s, 2H, SCH2), 6.82 (d, J=5.4 Hz, 1H), 7.12 (d, J=7.7 Hz, 1H), 7.24 (d, J=12.1 Hz, 1H), 8.28 (d, J=5.5 Hz, 1H); Mass (m/z) 439 (M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06051570
Source datasetuspto-grants-2000_04
ORD IDord-894933d3454b46df8b5a612aae6466ef
Source noteuspto-grants-2000_04