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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1953156Generated: November 5, 2026

Cyanogen Bromide → HCID 15888359, compound

https://huagongshe.com/reaction/1953156

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyanogen BromideHCID 10476—
ReactantHCID 11171593HCID 11171593—
SolventDichloromethaneHCID 6344—
ProductHCID 15888359HCID 1588835990.1%

Reaction Steps

To a cooled solution of 2-butylimidazo[1,2-d]-1,2,4-thiadiazole-3(2H)-one (4.78 g, 0.0242 mole) in 25 mL dichloromethane, cyanogen bromide (5.13 g, 0.0482 mole) was added in one portion and the mixture was stirred for 16 h at room temperature. The precipitate was filtered, slurried in 10 mL of methanol and subsequently washed with dichloromethane to give 4.45 g (90%) of 3-bromoimidazo[1,2-d]-1,2,4-thiadiazole as a colourless powder: mp 220° C. (dec); MS in/z 205, 203 (M+). Anal. Calcd for C4H2N3SBr.circle-solid.1/2 H2O: C, 22.55;H, 1.42; N, 19.72; O, 3.75; S, 15.02; Br, 37.50. Found: Cf 22.79;H, 1.41; N, 19.42; O, 2.67; S, 14.61; Br, 38.20.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06114537
Source datasetuspto-grants-2000_09
ORD IDord-0376a3cf5792455eaa345aacc816f439
Source noteuspto-grants-2000_09