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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2289590Generated: November 2, 2026

Phenylglyoxylonitrile → HCID 9838563, compound

https://huagongshe.com/reaction/2289590

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylglyoxylonitrileHCID 11953—
ReactantHCID 13034031HCID 13034031—
SolventDichloromethaneHCID 6344—
ProductHCID 9838563HCID 983856396%

Reaction Steps

A mixture of 2-butyl-1,2,4-thiadiazolo[4,5-a]benzimidazole-3(2H)-one (6.0 g, 24.3 mmole) and benzoyl cyanide (6.36 g, 48.5 mmole) in 80 mL of dichloromethane was stirred at room temperature for 24 h. The precipitate was filtered and washed with dichloromethane. The crude product was recrystallized from acetone to give 6.48 g (96%) of 3-(oxophenylmethyl)-1,2,4-thiadiazolo[4,5-a]benzimidazole as yellow crystals: mp 190-191° C.; 1H NMR (CDCl3) δ 8.35 (d, 3H), 7.82 (d, 1H), 7.73 (t, 1H), 7.59 (t, 2H), 7.50 (t, 1H), 7.36 (t, 1H) ppm; 13C NMR (CDCl3) δ180.86, 163.69, 150.82, 146.70, 134.79, 134.34, 131.22 (2C), 129.46 (2C), 128.74, 125.82, 122.27, 119.49, 115.23 ppm; IR (KBr) ν 1671 cm-1 ; HRMS calcd for C15H9N3OS: 279.0466, found: 279.0475. Anal. Calcd for C15H9N3OS: C, 64.50; H, 3.25; N, 15.04. Found: C, 63.93; H, 3.10; N, 14.53.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06093738
Source datasetuspto-grants-2000_07
ORD IDord-483d3e924274455fb82a9b49b94fc126
Source noteuspto-grants-2000_07