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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2289597Generated: November 1, 2026

Cyanogen Bromide → HCID 10198942, compound

https://huagongshe.com/reaction/2289597

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyanogen BromideHCID 10476—
ReactantHCID 13034031HCID 13034031—
SolventDichloromethaneHCID 6344—
ProductHCID 10198942HCID 1019894281.4%

Reaction Steps

A mixture of 2-butyl-1,2,4-thiadiazolo[4,5-a]benzimidazole-3(2H)-one (5.0 g, 20.2 mmole) and cyanogen bromide (4.28 g, 40.4 mmole) in 100 mL of dichloromethane was stirred at room temperature for 26 h. The precipitate was filtered and washed with dichloromethane to yield 4.18 g (81%) of 3 -bromo-1,2,4-thiadiazolo[4,5-a]benzimidazole as a white powder: mp 189-190 ° C.; 1H NMR (CDCl3) δ 8.23 (d, 1H), 7.82 (d, 1H), 7.52 (t, 1H), 7.42 (d, 1H) ppm; 13C NMR (1:1 CDCl3 :DMSO-d6) : δ 162.78, 149.67, 129.22, 125.53, 122.25, 119.48, 117.25, 111.27 ppm; IR (KBr) : ν 3025, 2925, 1601, 1493, 1451, 1028, 757, 701 cm-1 ; HRMS calcd for C8H4N3SBr 252.9309, found 252.9307. Anal. Calcd for C8H4N3SBr: C, 37.81; H, 1.59; N, 16.54. Found: C, 37.44; H, 1.33; N, 16.57.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06093738
Source datasetuspto-grants-2000_07
ORD IDord-e9a51a5dd457480882689389eb870bb8
Source noteuspto-grants-2000_07