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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 452061Generated: October 26, 2026

5-Aminobenzimidazole → HCID 178458237, compound

https://huagongshe.com/reaction/452061

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-AminobenzimidazoleHCID 13623—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactant4-PropoxybenzaldehydeHCID 79812—
ReactantTrimethylsilyl cyanideHCID 82115—
ProductHCID 178458237HCID 178458237—

Reaction Steps

The compound was synthesized starting from 5-aminobenzimidazole (0.585 g, 4.4 mmol), 4-propoxybenzaldehyde (0.632 mL, 4 mmol), TMSCN (0.5 mL, 4 mmol), PdC (10%, 0.02 g), TEA 0.558 mL, 4 mmol), di-(imidazol-1-yl)methanone (0.648, 4 mmol) as described in method 2. Yield: 0.135 g (10.0%); MS m/z 337.0 (M+H)+; 1H NMR (DMSO, 400 MHz): δ 0.90-0.93 (m, 3H); 1.61-1.70 (m, 2H); 3.08-3.12 (m, H); 3.81-3.87 (m, 3H); 5.49-5.53 (m, H); 6.85 (d, 2H, J=8.3 Hz); 7.19 (s, H); 7.25 (d, 2H, J=8.7 Hz); 7.55 (dd, H, 3J=9.1 Hz, 4J=2.1 Hz); 7.62 (d, H, J=9.1 Hz); 7.86 (d, H, 4J=2.1 Hz); 9.21 (s, H), HPLC (λ=214 nm, [B]: rt 9.00 min (99%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08486940B2
Source datasetuspto-grants-2013_07
ORD IDord-234c99225a1143989eeb799fddd87bc6
Source noteuspto-grants-2013_07