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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1488987Generated: November 2, 2026

Phenylglyoxylonitrile → HCID 9838563, compound

https://huagongshe.com/reaction/1488987

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) δ8.35 (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) ν1671 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 numberUS05677302
Source datasetuspto-grants-1997_10
ORD IDord-c85a2cdcd87b449da1b2643dbbf271f7
Source noteuspto-grants-1997_10